AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial

已完结 10 由 rui 发布于 2025/5/20 0:03:02

DOI:10.1016/s0140-6736(23)02874-x
作者：Jun Lv, Hui Wang, Xiaoting Cheng, Yuxin Chen, Daqi Wang, Longlong Zhang, Qi Cao, Honghai Tang, Shaowei Hu, Kaiyu Gao, Mengzhao Xun, Jinghan Wang, Zijing Wang, Biyun Zhu, Chong Cui, Ziwen Gao, Luo Guo,
文献类型：期刊论文
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Elsevier

Abstract：BackgroundAutosomal recessive deafness 9, caused by mutations of the OTOF gene, is characterised by congenital or prelingual, severe-to-complete, bilateral hearing loss. However, no pharmaco

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