A Novel GJB2 compound heterozygous mutation c.257C > G (p.T86R)/c.176del16 (p.G59A fs*18) causes sensorineural hearing loss in a Chinese family

Journal of Clinical Laboratory Analysis, EarlyView.

Source: Journal of Clinical Laboratory Analysis - April 17, 2018 Category: Laboratory Medicine Authors: Xi Shi , Yan Zhang , Shiwei Qiu , Wei Zhuang , Na Yuan , Tiantian Sun , Jian Gao , Yuehua Qiao , Ke Liu Source Type: research