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Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript

✍ Scribed by Yuval Ramot; Liran Horev; Irena Smolovich; Vered Molho-Pessach; Abraham Zlotogorski

Book ID: 111244643
Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 237 KB
Volume: 19
Category: Article
ISSN: 0906-6705
DOI: 10.1111/j.1600-0625.2009.01042.x

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## Background: Hypotrichosis of the marie unna type (hmu) is a rare autosomal dominant disorder characterized by male-pattern hair loss with childhood onset and anomalies of the hair shaft. ## Objectives: We aimed to evaluate a number of chromosomal loci as possible candidate regions for hmu. ##