A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp
Identifieur interne : 000306 ( France/Analysis ); précédent : 000305; suivant : 000307A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp
Auteurs : S. Nahum [Israël] ; F. Morice-Picard [France] ; A. Taieb [France] ; E. Sprecher [Israël]Source :
- Clinical and Experimental Dermatology [ 0307-6938 ] ; 2011-03.
Abstract
Background. Autosomal recessive hypotrichosis simplex (ARHS) presents with progressive hair loss mainly affecting the scalp area. In a small number of families, the condition has been associated with mutations in three distinct genes: DSG4, LIPH and LPAR6.
Url:
DOI: 10.1111/j.1365-2230.2010.03944.x
Affiliations:
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<front><div type="abstract">Background. Autosomal recessive hypotrichosis simplex (ARHS) presents with progressive hair loss mainly affecting the scalp area. In a small number of families, the condition has been associated with mutations in three distinct genes: DSG4, LIPH and LPAR6.</div>
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