Identification of a novelU2HRmutation in a Korean woman with Marie Unna hereditary hypotrichosis-Reference-Cited by-同舟云学术

Identification of a novelU2HRmutation in a Korean woman with Marie Unna hereditary hypotrichosis

Published:2014-06-25 Issue:11 Volume:53 Page:1358-1361
ISSN:0011-9059
Container-title:International Journal of Dermatology
language:en
Short-container-title:Int J Dermatol

Author:

Yun Seok-Kweon¹²,Cho Yong-Gon³,Song Ki Hun¹,Hwang Su-Ran¹,Kim Yoon Sung-Joo⁴,Choi Keon-Woo⁴,Kim Han-Uk¹²,Park Jin¹²

Affiliation:

1. Department of Dermatology; Chonbuk National University Medical School; Jeonju Korea

2. Research Institute of Clinical Medicine of Chonbuk National University-Biochemical Research Institute of Chonbuk National University Hospital; Jeonju Korea

3. Laboratory Medicine; Chonbuk National University Medical School; Jeonju Korea

4. Department of Medical Lifesciences; College of Medicine, The Catholic University of Korea; Seoul South Korea Korea

Publisher

Wiley

Subject

Dermatology

Reference17 articles.

1. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis;Wen;Nat Genet,2009

2. Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3;Yang;J Invest Dermatol,2005

3. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis;Lefevre;Eur J Hum Genet,2000

4. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family;Cichon;Br J Dermatol,2000

5. Marie Unna hereditary hypotrichosis gene maps to human chromosome 8p21 near hairless;Sreekumar;J Invest Dermatol,2000

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