A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family

We aimed to investigate the genetic causes of hearing loss in a Chinese proband with autosomal recessive congenital deafness.

Source: International Journal of Pediatric Otorhinolaryngology - May 29, 2017 Category: ENT & OMF Authors: Xiaoguang He, Qi Peng, Siping Li, Pengyuan Zhu, Chunqiu Wu, Chunbao Rao, Jingqi Lin, Xiaomei Lu Source Type: research