TTop stories Read More Multicentre gene therapy for OTOF-related deafness followed up to 2.5 yearsApril 23, 2026 Yasunaga, S. et al. A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form…
HHeadlines Read More TAU researchers develop groundbreaking gene therapy to treat hearing, balance disabilitiesNovember 10, 2025 “These findings highlight the potential of self-complementary AAVs to reduce dose requirements, minimize toxicity, and broaden clinical use…