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

作者：Xiaoguang He; Qi Peng; Siping Li; Pengyuan Zhu; Chunqiu Wu; Chunbao Rao; Jingqi Lin; Xiaomei Lu

来源：International Journal of Pediatric Otorhinolaryngology, 2017, 99: 40-43.

DOI：10.1016/j.ijporl.2017.05.021

• Usher syndrome
• Hearing loss
• MYO7A
• Novel mutation

Objectives

• 出版日期2017-8