Open AccessCase report: Novel GJB2 variant c.113T>C associated with autosomal recessive non-syndromic hearing loss (ARNSHL) in a Han family
Author(s) -
Xinqiang Lan,
Shiyu Sun,
Lan X,
L. C. Niu,
Chunxiao Zhang,
Xiaoli Chen,
Ningning Xia
Publication year - 2019
Publication title -
medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 148
eISSN - 1536-5964
pISSN - 0025-7974
DOI - 10.1097/md.0000000000018253
Subject(s) - medicine , hearing loss , genetic counseling , genetic testing , mutation , genetics , gene , psychological intervention , bioinformatics , audiology , biology , psychiatry
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