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A recurrent mutation in the KRT 17 gene responsible for severe steatocystoma multiplex in a large Chinese family
Author(s) -
Wang J.,
Li J.,
Li X.,
Lei D.,
Xiao W.,
Li Z.,
Zhang S.,
Li M.
Publication year - 2018
Publication title -
clinical and experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 78
eISSN - 1365-2230
pISSN - 0307-6938
DOI - 10.1111/ced.13311
Subject(s) - mutation , genetics , gene , multiplex , biology , medicine