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A novel deletion mutation in the phospholipase H ( LIPH ) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2)
Author(s) -
KamranulHassan Naqvi S.,
Raza S.I.,
Naveed A.K.,
John P.,
Ahmad W.
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.1365-2133.2008.08822.x
Subject(s) - medicine , biology , genetics , library science , computer science