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A frameshift mutation of TMPRSS3 in a Chinese family with non-syndromic hearing loss

BackgroundDeafness 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).ObjectivesTo identify clinically relevant gene variants associated with NSHL in a Chinese family using trio-base...

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Main Authors:	Jingwen Liang (Author), Zhuoheng Yu (Author), Zhangxing Wang (Author), Jianxia Chen (Author), Yihuan Liu (Author), Zhaoqing Yin (Author), Ruihuan Xu (Author)
Format:	Book
Published:	Frontiers Media S.A., 2022-12-01T00:00:00Z.
Subjects:	article
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