我国科研人员在基因治疗耳聋研究方面取得新突破

Core Viewpoint - Researchers in China have made significant breakthroughs in gene therapy for hereditary deafness, with findings published in the prestigious journal Nature Medicine, indicating the potential of adeno-associated virus gene therapy for autosomal recessive hereditary hearing loss, which could provide hope for millions of patients worldwide [1] Group 1 - The research was conducted by Professor Chai Renjie from the Ear, Nose, Throat, and Head and Neck Surgery Department at Southeast University Affiliated Zhongda Hospital, in collaboration with multiple institutions [1] - The findings reveal the important clinical guidance value of this gene therapy approach, suggesting it could enable millions of hereditary deafness patients to "hear the world" [1]