Open AccessThe Clinical Manifestation of p.Asp50Asn Heterozygous Mutation of GJB2 Gene in 3 Members of a Family Is Similar to That of Clouston Syndrome
Author(s) -
Yanjiang Xu,
Minhua Wang,
Huang Ling,
Jie Hu
Publication year - 2022
Publication title -
annals of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.385
H-Index - 37
eISSN - 2005-3894
pISSN - 1013-9087
DOI - 10.5021/ad.20.278
Subject(s) - photophobia , medicine , proband , hyperkeratosis , dermatology , ichthyosis , daughter , hearing loss , family history , genetics , mutation , audiology , surgery , gene , evolutionary biology , biology
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