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A novel point mutation of keratin 17 ( KRT17 ) in a Japanese family with pachyonychia congenita type 2: an RNA‐based genetic analysis using a single hair bulb
Author(s) -
Tsuda T.,
Ishikawa C.,
Nakagawa N.,
Konishi H.,
Tarutani M.,
Matsuki M.,
Yamanishi K.
Publication year - 2008
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.1365-2133.2008.08684.x
Subject(s) - medicine , dermatology