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Three‐base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease
Author(s) -
Tsuruta D.,
Akiyama M.,
IshidaYamamoto A.,
Imanishi H.,
Mizuno N.,
Sowa J.,
Kobayashi H.,
Ishii M.,
Kurokawa I.,
Shimizu H.
Publication year - 2010
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.1365-2133.2009.09580.x
Subject(s) - darier disease , darier's disease , biology , pathology , phenotype , mutation , hyperkeratosis , disease , medicine , genetics , gene