Marie Unna hereditary hypotrichosis: a recurrent c.74C>T mutation in theU2HRgene and literature review
Author:
Affiliation:
1. Department of Dermatology; Second Affiliated Hospital; Zhejiang University School of Medicine; Hangzhou China
2. Department of Dermatology; Nanfang Hospital; Southern Medical University; Guangzhou China
Publisher
Wiley
Subject
Dermatology
Reference10 articles.
1. Identification of a novel U2HR mutation c.14C>T in a Chinese patient with Marie Unna hereditary hypotrichosis;Zhou;Eur J Dermatol,2011
2. Hypotrichosis congenita hereditaria;Uber;Dermatol Wochenschr,1925
3. Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis;Düzenli;Clin Exp Dermatol,2009
4. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis;Wen;Nat Genet,2009
5. The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing;Steensel;Am J Hum Genet,1999
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