Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference12 articles.
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2. G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth;SM Pasternack;Nat Genet,2008
3. A novel phosphatidic acid-selective phospholipase A1 that produces lysophosphatidic acid;H Sonoda;J Biol Chem,2002
4. In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth;SM Pasternack;J Invest Dermatol,2009
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1. Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient;Frontiers in Medicine;2024-05-16
2. Molecular Basis of Hereditary Hair Diseases;The Keio Journal of Medicine;2023
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4. Update of recent findings in genetic hair disorders;The Journal of Dermatology;2021-10-21
5. Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies;Journal of the European Academy of Dermatology and Venereology;2021-06-04
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