Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis-Reference-Cited by-同舟云学术

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Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis

Published:2013-01-07 Issue:4 Volume:40 Page:278-280
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Ito Taisuke¹,Shimomura Yutaka²,Ogai Masaaki³,Sakabe Jun-Ichi¹,Tokura Yoshiki¹

Affiliation:

1. Department of Dermatology; Hamamatsu University School of Medicine; Hamamatsu; Japan

2. Laboratory of Genetic Skin Diseases; Niigata University Graduate School of Medical and Dental Sciences; Niigata; Japan

3. Department of Dermatology; Seirei Hamamatsu General Hospital; Hamamatsu; Japan; Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Reference5 articles.

1. Overexpression of Hr links excessive induction of Wnt signaling to Marie Unna hereditary hypotrichosis;Kim;Hum Mol Genet,2012

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

3. Uber hypotrichosis congenita hereditaria;Unna;Dermatol Wochenschr,1925

4. A novel U2HR non-synonymous mutation in a Chinese patient with Marie Unna hereditary hypotrichosis;Cai;J Dermatol Sci,2009

5. Alopecia universalis associated with a mutation in the human hairless gene;Ahmad;Science,1998

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Update of recent findings in genetic hair disorders;The Journal of Dermatology;2021-10-21

2. Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report;European Journal of Dermatology;2018-05

3. Hereditary Hair Diseases (part 1);Nishi Nihon Hifuka;2018-04-01

4. Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family;The Journal of Dermatology;2017-04-13

5. Identification of mutations inU2HRin two Chinese families with Marie Unna hereditary hypotrichosis;Clinical and Experimental Dermatology;2015-08-12

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