Identification of mutations inU2HRin two Chinese families with Marie Unna hereditary hypotrichosis-Reference-Cited by-同舟云学术

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Identification of mutations inU2HRin two Chinese families with Marie Unna hereditary hypotrichosis

Published:2015-08-12 Issue:2 Volume:41 Page:175-178
ISSN:0307-6938
Container-title:Clinical and Experimental Dermatology
language:en
Short-container-title:Clin Exp Dermatol

Author:

Zhong Z.¹²³,Zhong M.⁴,Lu Y.¹²³,Lu L.¹²,Wang J.¹²,Xu D.¹,Wang F.¹,Xu G.¹²,Chen J.¹²³

Affiliation:

1. Department of Ophthalmology of Shanghai Tenth People's Hospital and Tongji Eye Institute; Tongji University School of Medicine; Shanghai China

2. Department of Regenerative Medicine and Stem Cell Research Center; Tongji University School of Medicine; Shanghai China

3. Department of Medical Genetics; Tongji University School of Medicine; Shanghai China

4. Department of Ophthalmology of Pingxiang People's Hospital; Pingxiang Jiangxi China

Funder

National High Technology Research and Development Program of China

National Natural Science Foundation of China

Thousand Young Talents programme of China

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ced.12711/fullpdf

Reference10 articles.

1. Marie Unna hereditary hypotrichosis;Argenziano;Eur J Dermatol,1999

2. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3;He;Br J Dermatol,2004

3. 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

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. Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis;Düzenli;Clin Exp Dermatol,2009

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