A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2)
- 15 December 2008
- journal article
- case report
- Published by Wiley in British Journal of Dermatology
- Vol. 160 (1), 194-196
- https://doi.org/10.1111/j.1365-2133.2008.08822.x
Abstract
No abstract availableKeywords
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