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Article

Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.

The British journal of dermatology - 1 May 2009

Tariq M, Ayub M, Jelani M, Basit S, Naz G, Wasif N, Raza S I, Naveed A K, ullah Khan S, Azeem Z, Yasinzai M, Wali A, Ali G, Chishti M S, Ahmad W

Abstract excerpt

BACKGROUND: Autosomal recessive hypotrichosis is a rare genetic irreversible hair loss characterized by sparse scalp hair, sparse to absent eyebrows and eyelashes, and sparse axillary and body hair. Affected male individuals have normal beard hair. OBJECTIVES: To search for pathogenic mutations in the human P2RY5 gene in Pakistani families with autosomal recessive hereditary hypotrichosis. METHODS: In the present...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19292720
DOI: 10.1111/j.1365-2133.2009.09046.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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