Mutations in the LIPH gene in three Japanese families with autosomal recessive woolly hair/hypotrichosis
Author:
Publisher
Elsevier BV
Subject
Dermatology,Molecular Biology,Biochemistry
Reference10 articles.
1. Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH;Kazantseva;Science,2006
2. Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair;Shimomura;Nat Genet,2008
3. Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis;Shimomura;J Invest Dermatol,2009
4. A novel phosphatidic acid-selective phospholipase A1 that produces lysophosphatidic acid;Sonoda;J Biol Chem,2002
5. Identification and characterization of a novel lysophosphatidic acid receptor, p2y5/LPA6;Yanagida;J Biol Chem,2009
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1. A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies;Journal of Investigative Dermatology;2023-01
2. Lysophospholipid Mediators in Health and Disease;Annual Review of Pathology: Mechanisms of Disease;2022-01-24
3. Update of recent findings in genetic hair disorders;The Journal of Dermatology;2021-10-21
4. Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies;Journal of the European Academy of Dermatology and Venereology;2021-06-04
5. Trichoscopy in Hair Shaft Disorders;Dermatologic Clinics;2018-10
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