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Article

Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair

24 Feb 2008

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18297072
DOI: 10.1038/ng.100

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Related research

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Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hairPMID 18297072Read ↗

Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.Semantic proximity Read ↗

Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation.Semantic proximity Read ↗

Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair.Semantic proximity Read ↗

A novel deletion mutation in P2RY5/LPA(6) gene cause autosomal recessive woolly hair with hypotrichosis.Semantic proximity Read ↗

[Of hair and genes: The continuing story of Dowling-Degos disease].Semantic proximity Read ↗

Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.Semantic proximity Read ↗

A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies.Semantic proximity Read ↗

The Polygenic Architecture of Human Diseases Affecting the Hair Follicle.Semantic proximity Read ↗

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Genetic hair loss.Semantic proximity Read ↗

Mutations in LPAR6/P2RY5 and LIPH are associated with woolly hair and/or hypotrichosis.Semantic proximity Read ↗

Current insight into the functions of microRNAs in common human hair loss disorders: a mini reviewSemantic proximity Read ↗

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