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Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C‐terminus of KIT
Author(s) -
Takeichi T.,
Sugiura K.,
Tanahashi K.,
Noda K.,
Kono M.,
Akiyama M.
Publication year - 2018
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.16895
Subject(s) - missense mutation , hyperpigmentation , medicine , mutation , genetics , dermatology , pigmentation disorder , biology , gene