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Association of Cole disease with novel heterozygous mutations in the somatomedin‐B domains of the ENPP 1 gene: necessary, but not always sufficient
Author(s) -
Schlipf N.A.,
Traupe H.,
Gilaberte Y.,
Peitsch W.K.,
Hausser I.,
Oji V.,
Schmieder A.,
Schneider S.W.,
Demmer P.,
Rösler B.,
Fischer J.
Publication year - 2016
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/bjd.14328
Subject(s) - gene , genetics , mutation , biology , somatomedin , medicine , growth factor , receptor
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