Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families
Yi Zhu, Yaping Qian, Xiaowen Tang, Jindan Wang, Li Yang, Zhisu Liao, Ronghua Li, Jinzhang Ji, Zhiyuan Li, Jian‐Fu Chen, Daniel I. Choo, Jianxin Lü, Min‐Xin Guan
Abstract