{"id":1007436,"date":"2026-10-01T08:25:38","date_gmt":"2026-10-01T12:25:38","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/"},"modified":"2026-10-01T08:25:38","modified_gmt":"2026-10-01T12:25:38","slug":"taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/","title":{"rendered":"Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting"},"content":{"rendered":"<div class=\"mw_release\">\n<p>DALLAS, Oct.  01, 2026  (GLOBE NEWSWIRE) &#8212; Taysha Gene Therapies, Inc. (Nasdaq: TSHA) (Taysha or the Company), a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system (CNS), today announced multiple encore presentations supporting its TSHA-102 program in clinical evaluation for Rett syndrome at the 55<sup>th<\/sup> Child Neurology Society Annual Meeting, taking place in\u00a0Montr\u00e9al, Qu\u00e9bec, Canada, from\u00a0October 14 \u2013 17, 2026.<\/p>\n<p>The presentations will highlight data previously shared at the 2026 International Rett Syndrome Foundation (IRSF) Scientific Meeting. IRSF poster presentations are available on Taysha\u2019s\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=AEdTTk0ntx9tGH8mVpKEQm2bR_yXL0ntkShFWY9jfYOBV840l7b64DfM-3zb33K8j0MsdxMXBDcuMQexTnDeYMP2PTyEcbYcBkTfYuhrqsLaaBROqN2cCkju2LcE50XF\" rel=\"nofollow\" target=\"_blank\">website<\/a>.<\/p>\n<p>\n        <strong><br \/>\n          <u>Oral Presentation:<\/u><br \/>\n        <\/strong><br \/>\n        <br \/>\n        <strong>Title: <\/strong>Multi-Domain Functional Gains Following TSHA-102 Gene Therapy Across the Rett Syndrome Lifespan: Safety and Efficacy Results from the REVEAL Part A Phase 1\/2 Trial of TSHA-102 in Pediatric and Adolescent\/Adult Cohorts<br \/><strong>Date\/Time: <\/strong>Thursday, October 15, 2026, 12:30\u20131:45 PM ET <br \/><strong>Presenter: <\/strong>Elsa Rossignol, M.D., FRCP, FAAP, Professor in Neuroscience and Pediatrics at the Universit\u00e9 de Montr\u00e9al, Director of the Rett Multidisciplinary Clinic of the CHU Sainte-Justine and a Principal Investigator of the REVEAL trial<\/p>\n<p>\n        <strong><br \/>\n          <u>Poster Presentations:<\/u><br \/>\n        <\/strong><br \/>\n        <br \/>Posters will be presented on Thursday, October 15, from 12:30\u20131:45 PM ET and from 5:30\u20137:00 PM ET.<\/p>\n<p>\n        <strong>Title: <\/strong>The Developmental Plateau in Rett Syndrome: New Insights from the Natural History Study Inform Novel Interventional Study Designs<br \/><strong>Poster Number: <\/strong>262<br \/><strong>Presenter: <\/strong>Minna Montgomery, Medical Office Chief of Staff and Head of Program Management Office, Taysha Gene Therapies<\/p>\n<p>\n        <strong>Title: <\/strong>Establishing the Rett Syndrome Developmental Milestone Assessment (RS-DMA) as a Primary Endpoint for Interventional Studies <br \/><strong>Poster Number: <\/strong>272<br \/><strong>Presenter: <\/strong>Tessa Clarkson, Ph.D., Co-Founder and CEO, Psychlomere, LLC<\/p>\n<p>\n        <strong>Title: <\/strong>Multi-Domain Functional Gains Following TSHA-102 Gene Therapy Across the Rett Syndrome Lifespan: Safety and Efficacy Results from the REVEAL Part A Phase 1\/2 Trial of TSHA-102 in Pediatric and Adolescent\/Adult Cohorts<br \/><strong>Poster Number: <\/strong>264<br \/><strong>Presenter: <\/strong>Jason Cataldo, D.O., Vice President, Clinical Development and Safety Science, Taysha Gene Therapies<\/p>\n<p>\n        <strong><br \/>\n          <u>Company-Hosted Symposium:<\/u><br \/>\n        <\/strong><br \/>\n        <br \/>\n        <strong>Title: <\/strong>Rett Syndrome Across the Disease Continuum: From Natural History to Patient-Centered Innovation<br \/><strong>Date\/Time: <\/strong>Friday, October 16, 2026, 12:00\u20131:00 PM ET <br \/><strong>Presenters: <\/strong><\/p>\n<ul type=\"disc\">\n<li>Elsa Rossignol, M.D., FRCP, FAAP, Professor in Neuroscience and Pediatrics at the Universit\u00e9 de Montr\u00e9al, Director of the Rett Multidisciplinary Clinic of the CHU Sainte-Justine and a Principal Investigator of the REVEAL trial<\/li>\n<li>Jeffrey Neul, M.D., Ph.D., Director, Vanderbilt Kennedy Center, Annette Schaffer Eskind Chair, Professor at the Vanderbilt University Medical Center, who served as Administrative Head of the Rett Syndrome Natural History Study<\/li>\n<li>Tessa Clarkson, Ph.D., Co-Founder and CEO, Psychlomere, LLC<\/li>\n<\/ul>\n<p>\n        <strong>About TSHA-102<\/strong><br \/>\n        <br \/>TSHA-102 is a self-complementary intrathecally delivered AAV9 investigational gene transfer therapy in clinical evaluation for Rett syndrome. Designed as a one-time treatment, TSHA-102 aims to address the genetic root cause of the disease by delivering a functional form of\u00a0<em>MECP2<\/em>\u00a0to cells in the CNS. TSHA-102 utilizes a novel miRNA-Responsive Auto-Regulatory Element (miRARE) technology designed to mediate levels of\u00a0<em>MECP2<\/em>\u00a0in the CNS on a cell-by-cell basis without risk of overexpression. TSHA-102 has received Breakthrough Therapy, Regenerative Medicine Advanced Therapy,\u00a0Fast Track\u00a0and Orphan Drug and Rare Pediatric Disease designations from the FDA, Orphan Drug designation from the\u00a0European Commission\u00a0and\u00a0Innovative Licensing\u00a0and Access Pathway designation from the Medicines and Healthcare products Regulatory Agency.<\/p>\n<p>\n        <strong>About Rett Syndrome<\/strong><br \/>\n        <br \/>Rett syndrome is a rare neurodevelopmental disorder caused by mutations in the X-linked\u00a0<em>MECP2<\/em>\u00a0gene encoding methyl CpG-binding protein 2 (MeCP2), which is essential for regulating neuronal and synaptic function in the brain. The disorder is characterized by loss of communication and hand function, slowing and\/or regression of development, motor and respiratory impairment, seizures, intellectual disabilities and shortened life expectancy. Rett syndrome progression is divided into four key stages, beginning with early onset stagnation at 6 to 18 months of age followed by rapid regression, plateau and late motor deterioration. Rett syndrome primarily occurs in females and is one of the most common genetic causes of severe intellectual disability. Currently, there are no approved disease-modifying therapies that treat the genetic root cause of the disease. Rett syndrome caused by a pathogenic\/likely pathogenic <em>MECP2 <\/em>mutation is estimated to affect between 15,000 and 20,000 patients in the\u00a0U.S., EU, and\u00a0U.K.<\/p>\n<p>\n        <strong>About\u00a0Taysha Gene Therapies<\/strong><br \/>\n        <br \/>Taysha Gene Therapies\u00a0(Nasdaq: TSHA) is a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system. Its lead clinical program TSHA-102 is in development for Rett syndrome, a rare neurodevelopmental disorder with no approved disease-modifying therapies that address the genetic root cause of the disease. With a singular focus on developing transformative medicines, Taysha aims to address severe unmet medical needs and dramatically improve the lives of patients and their caregivers. The Company\u2019s management team has proven experience in gene therapy development and commercialization. Taysha leverages this experience, its manufacturing process and a clinically and commercially proven AAV9 capsid in an effort to rapidly translate treatments from bench to bedside. For more information, please visit\u202f<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=cwYYdzFY1XwZ43Hc5wn8UmM7n9c9ubhVkjV1GTo5UcFLENrZnPOlvsKKTHQalbANX7YFC1Fe6_FyEsd8QAlPK7zB1ZF7FHtJ7zG1zs6OFXA=\" rel=\"nofollow\" target=\"_blank\">www.tayshagtx.com<\/a>.<\/p>\n<p>\n        <strong>Company Contact:<\/strong><br \/>\n        <br \/>\n        <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=nIyHR6cgeqaIGAoQ3lewQr6_JMlLx0DVbCwbuXfwOmSL_7Kgi_HAB3S91zcUnADxb4dquqelJpvUbRt7Vh8Hi-ZQcj0sUlqThT2LSAZl2HIkqnRrDlgyrS_KnmYNoBFz\" rel=\"nofollow\" target=\"_blank\">investors@tayshagtx.com<\/a>\n      <\/p>\n<p>\n        <strong>Media Contact:<\/strong><br \/>\n        <br \/>\n        <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=Dnc2AlBH8lT14Khia1_a0GeXfGoA8ArmAP79eucd8vSeo_M53mBuHa8eQczL85i1ZX2sHKhsiqQBRIZ-nhCLXnwI_ocWWoFBZUYrdPLP_MkEsATLcFK-EsDIr88nr1vvp6oSXDWhVJcXSXe95KqwHixAVcc28cvRjkXaROA_6J75xVMe0QRa70Xzl4c6F7d5qMGossJ8bBuHgqosSAqk9_Fqin4jeStVY_1tbucBMlM-ifEF_pqMKD1zS22sgcA6gZtkZ6Hj_wUL42iGdIN_mQ==\" rel=\"nofollow\" target=\"_blank\">media@tayshagtx.com<\/a>\n      <\/p>\n<p>      <img decoding=\"async\" alt=\"\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTgzNzMzNCM3ODcyOTYyIzIyMDI0MTM=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/MThjYTYzNjYtNmUwYy00MjliLTlhYjEtMjI1YTkwNmEzNTI4LTEyMTM5NjYtMjAyNi0xMC0wMS1lbg==\/tiny\/Taysha-Gene-Therapies-Inc-.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>DALLAS, Oct. 01, 2026 (GLOBE NEWSWIRE) &#8212; Taysha Gene Therapies, Inc. (Nasdaq: TSHA) (Taysha or the Company), a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system (CNS), today announced multiple encore presentations supporting its TSHA-102 program in clinical evaluation for Rett syndrome at the 55th Child Neurology Society Annual Meeting, taking place in\u00a0Montr\u00e9al, Qu\u00e9bec, Canada, from\u00a0October 14 \u2013 17, 2026. The presentations will highlight data previously shared at the 2026 International Rett Syndrome Foundation (IRSF) Scientific Meeting. IRSF poster presentations are available on Taysha\u2019s\u00a0website. Oral Presentation: Title: Multi-Domain Functional Gains Following TSHA-102 Gene Therapy Across the Rett Syndrome Lifespan: Safety and Efficacy Results from the REVEAL Part A &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-1007436","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"DALLAS, Oct. 01, 2026 (GLOBE NEWSWIRE) &#8212; Taysha Gene Therapies, Inc. (Nasdaq: TSHA) (Taysha or the Company), a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system (CNS), today announced multiple encore presentations supporting its TSHA-102 program in clinical evaluation for Rett syndrome at the 55th Child Neurology Society Annual Meeting, taking place in\u00a0Montr\u00e9al, Qu\u00e9bec, Canada, from\u00a0October 14 \u2013 17, 2026. The presentations will highlight data previously shared at the 2026 International Rett Syndrome Foundation (IRSF) Scientific Meeting. IRSF poster presentations are available on Taysha\u2019s\u00a0website. Oral Presentation: Title: Multi-Domain Functional Gains Following TSHA-102 Gene Therapy Across the Rett Syndrome Lifespan: Safety and Efficacy Results from the REVEAL Part A &hellip; Continue reading &quot;Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-10-01T12:25:38+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTgzNzMzNCM3ODcyOTYyIzIyMDI0MTM=\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"4 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting\",\"datePublished\":\"2026-10-01T12:25:38+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\\\/\"},\"wordCount\":836,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=OTgzNzMzNCM3ODcyOTYyIzIyMDI0MTM=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\\\/\",\"name\":\"Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting - 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Market Newsdesk","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/","og_locale":"en_US","og_type":"article","og_title":"Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting - Market Newsdesk","og_description":"DALLAS, Oct. 01, 2026 (GLOBE NEWSWIRE) &#8212; Taysha Gene Therapies, Inc. (Nasdaq: TSHA) (Taysha or the Company), a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system (CNS), today announced multiple encore presentations supporting its TSHA-102 program in clinical evaluation for Rett syndrome at the 55th Child Neurology Society Annual Meeting, taking place in\u00a0Montr\u00e9al, Qu\u00e9bec, Canada, from\u00a0October 14 \u2013 17, 2026. The presentations will highlight data previously shared at the 2026 International Rett Syndrome Foundation (IRSF) Scientific Meeting. IRSF poster presentations are available on Taysha\u2019s\u00a0website. Oral Presentation: Title: Multi-Domain Functional Gains Following TSHA-102 Gene Therapy Across the Rett Syndrome Lifespan: Safety and Efficacy Results from the REVEAL Part A &hellip; Continue reading \"Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/","og_site_name":"Market Newsdesk","article_published_time":"2026-10-01T12:25:38+00:00","og_image":[{"url":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTgzNzMzNCM3ODcyOTYyIzIyMDI0MTM=","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"4 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting","datePublished":"2026-10-01T12:25:38+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/"},"wordCount":836,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/#primaryimage"},"thumbnailUrl":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTgzNzMzNCM3ODcyOTYyIzIyMDI0MTM=","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/taysha-gene-therapies-announces-multiple-encore-presentations-supporting-tsha-102-rett-syndrome-clinical-program-at-the-55th-child-neurology-society-annual-meeting\/","name":"Taysha Gene Therapies Announces Multiple Encore Presentations Supporting TSHA-102 Rett Syndrome Clinical Program at the 55th Child Neurology Society Annual Meeting - 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