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A Japanese piebald patient with auburn hair colour associated with a novel mutation p.P832L in the KIT gene and a homozygous variant p.I120T in the MC1R gene
Author(s) -
Oiso N.,
Kishida K.,
Fukai K.,
Motokawa T.,
Hosomi N.,
Suzuki T.,
Mitsuhashi Y.,
Tsuboi R.,
Kawada A.
Publication year - 2009
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/j.1365-2133.2009.09138.x
Subject(s) - forehead , melanocortin 1 receptor , genodermatosis , dermatology , scalp , trunk , medicine , genetics , anatomy , biology , allele , gene , ecology