Literature DB >> 26273173

A Case of Sporadic Dyschromatosis Universalis Hereditaria.

Je Min An1, Bum Joon Ko1, Moon Kyun Cho1, Kyu Uang Whang1.   

Abstract

Entities:  

Year:  2015        PMID： 26273173      PMCID： PMC4530167          DOI： 10.5021/ad.2015.27.4.467

Source DB:  PubMed          Journal:  Ann Dermatol        ISSN： 1013-9087            Impact factor:   1.444


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  4 in total

1.  Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family.

Authors:  I A Bukhari; E A El-Harith; M Stuhrmann
Journal:  J Eur Acad Dermatol Venereol       Date:  2006-05       Impact factor: 6.166

2.  Dyschromatosis universalis hereditaria.

Authors:  G Sethuraman; C R Srinivas; M D'Souza; D Mohan Thappa; L Smiles
Journal:  Clin Exp Dermatol       Date:  2002-09       Impact factor: 3.470

3.  Dyschromatosis universalis hereditaria: an electron microscopic examination.

Authors:  N S Kim; S Im; S C Kim
Journal:  J Dermatol       Date:  1997-03       Impact factor: 4.005

4.  Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.

Authors:  Hong Liu; Yi Li; Ken Kwok Hon Hung; Na Wang; Chuan Wang; Xuechao Chen; Donglai Sheng; Xi'an Fu; Kelvin See; Jia Nee Foo; Huiqi Low; Herty Liany; Ishak Darryl Irwan; Jian Liu; Baoqi Yang; Mingfei Chen; Yongxiang Yu; Gongqi Yu; Guiye Niu; Jiabao You; Yan Zhou; Shanshan Ma; Ting Wang; Xiaoxiao Yan; Boon Kee Goh; John E A Common; Birgitte E Lane; Yonghu Sun; Guizhi Zhou; Xianmei Lu; Zhenhua Wang; Hongqing Tian; Yuanhua Cao; Shumin Chen; Qiji Liu; Jianjun Liu; Furen Zhang
Journal:  PLoS One       Date:  2014-02-03       Impact factor: 3.240
  4 in total

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