A frameshift mutation of TMPRSS3 in a Chinese family with non-syndromic hearing loss
Jingwen Liang, Zhuoheng Yu, Zhangxing Wang, Jianxia Chen et autres
Background Deafness is the most common sensory defect in humans worldwide. Approximately 50% of cases are attributed to genetic factors, and about 70% are non-syndromic hearing loss (NSHL). Objectives To identify clinically relevant gene variants associated with NSHL in a Chinese family …
cn (code pays fourni par la source)
2 citations
Frontiers in Pediatrics