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Familial progressive hyper‐ and hypopigmentation caused by a novel mutation in site II of the KITLG gene
Author(s) -
Liu Zhenfeng,
Zhu Zhenlai,
Luo Junjie,
Yang Bin
Publication year - 2021
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 - 10.1111/1346-8138.16016
Subject(s) - hypopigmentation , mutation , genetics , gene , medicine , biology
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