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Identification of a founder mutation in KRT 14 associated with Naegeli–Franceschetti–Jadassohn syndrome
Author(s) -
Ralser D.J.,
Kumar S.,
Borisov O.,
Sarig O.,
Richard G.,
Wolf S.,
Krawitz P.M.,
Sprecher E.,
Kreiß M.,
Betz R.C.
Publication year - 2020
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.19123
Subject(s) - identification (biology) , mutation , medicine , founder effect , genetics , biology , gerontology , genotype , gene , haplotype , botany