{"id":32827,"date":"2025-07-02T14:47:19","date_gmt":"2025-07-02T14:47:19","guid":{"rendered":"https:\/\/www.europesays.com\/us\/32827\/"},"modified":"2025-07-02T14:47:19","modified_gmt":"2025-07-02T14:47:19","slug":"aav-gene-therapy-for-autosomal-recessive-deafness-9-a-single-arm-trial","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/us\/32827\/","title":{"rendered":"AAV gene therapy for autosomal recessive deafness 9: a single-arm trial"},"content":{"rendered":"<li class=\"c-article-references__item js-c-reading-companion-references-item\" data-counter=\"1.\">\n<p class=\"c-article-references__text\" id=\"ref-CR1\">Chang, Q. et al. Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome. EMBO Mol. 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