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Identification of a novel mutation in the LOR gene in an Iraqi patient with loricrin keratoderma resembling epidermolytic hyperkeratosis
Author(s) -
Khalil S.,
Daou L.,
Hayashi R.,
Abbas O.,
Nemer G.,
Saadeh D.,
Shimomura Y.,
Kurban M.
Publication year - 2017
Publication title -
journal of the european academy of dermatology and venereology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 107
eISSN - 1468-3083
pISSN - 0926-9959
DOI - 10.1111/jdv.13882
Subject(s) - medicine , keratoderma , dermatology , african american , family medicine , hyperkeratosis , anthropology , sociology
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