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Multicentre gene therapy for OTOF -related deafness followed up to 2.5 years - Nature

In a multicentre trial of AAV1-hOTOF gene therapy involving 42 participants aged 0.8–32.3 years with autosomal recessive deafness 9, treatment demonstrated safety, tolerability, and improved hearing a...

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  • Yasunaga, S. et al. A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness. Nat. Genet.21, 363369 (1999). Article  CAS  PubMed  Google S… [+7342 chars]
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