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Article

Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.

The British journal of dermatology - 1 May 2004

He P P, Zhang X J, Yang Q, Li M, Liang Y H, Yang S, Yan K L, Cui Y, Shen Y Y, Wang H Y, Sun L D, Du W H, Shen Y J, Xu S J, Huang W

Abstract excerpt

BACKGROUND: Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal congenital alopecia with progressive hair loss starting in early childhood and accelerating at puberty. A locus for MUHH has been mapped on chromosome 8p21 but no genes for MUHH have been identified to date. OBJECTIVES: To refine the MUHH locus to a narrow chromosome region to facilitate cloning of the gene. METHODS: We performed...

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Identifiers

PMID: 15149494
DOI: 10.1111/j.1365-2133.2004.05913.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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