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Classical Vohwinkel syndrome with heterozygous p.Asp66His mutation in GJB2 gene: Second Asian case
Author(s) -
Ikeda Kenta,
Takeichi Takuya,
Ito Yasutoshi,
Kawakami Yoshio,
Nakagawa Yuki,
Naito Seiko,
Yamasaki Osamu,
Akiyama Masashi,
Morizane Shin
Publication year - 2020
Publication title -
the journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 65
eISSN - 1346-8138
pISSN - 0385-2407
DOI - 10.1111/1346-8138.15513
Subject(s) - mutation , genetics , content (measure theory) , gene , physics , computer science , psychology , biology , mathematics , mathematical analysis
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