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A novel 3017‐bp deletion mutation in the FERMT1 ( KIND1 ) gene in a Chinese family with Kindler syndrome
Author(s) -
Zhou C.,
Song S.,
Zhang J.
Publication year - 2009
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.1365-2133.2009.09052.x
Subject(s) - poikiloderma , exon , genodermatosis , point mutation , gene , mutation , integrin , genetics , biology , medicine , microbiology and biotechnology , cancer research , cell