Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference26 articles.
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2. Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin;Levy-Nissenbaum;Nat Genet,2003
3. G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth;Pasternack;Nat Genet,2008
4. Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3);Azeem;Hum Genet,2008
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2. The constraints of racialization: How classification and valuation hinder scientific research on human variation;American Journal of Physical Anthropology;2021-03-05
3. Unusual Clinical Presentation of Autosomal Recessive Woolly Hair;Skin Appendage Disorders;2020
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5. Trichoscopy in Hair Shaft Disorders;Dermatologic Clinics;2018-10
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