Literature DB >> 14950856

Genetical studies on skin diseases. VII. Dyschromatosis universalis hereditaria in 5 generations.

M SUENAGA.   

Abstract

Entities:  

Keywords:  PIGMENTATION

Mesh：

Year:  1952        PMID： 14950856     DOI： 10.1620/tjem.55.373

Source DB:  PubMed          Journal:  Tohoku J Exp Med        ISSN： 0040-8727            Impact factor:   1.848


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  3 in total

1.  Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.

Authors:  Zhi-Qiang Wang; Lizhen Si; Quan Tang; Debao Lin; Zhangjie Fu; Jing Zhang; Bin Cui; Yufei Zhu; Xianghua Kong; Min Deng; Yu Xia; Heng Xu; Weidong Le; Landian Hu; Xiangyin Kong
Journal:  Am J Hum Genet       Date:  2009-04-16       Impact factor: 11.025

2.  Reticulate acropigmentation of dohi: a case report with insight into genodermatoses with mottled pigmentation.

Authors:  Deepak Mohana; Ujjwala Verma; Amarkant Jha Amar; R K P Choudhary
Journal:  Indian J Dermatol       Date:  2012-01       Impact factor: 1.494

3.  Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria.

Authors:  Ying-Xia Cui; Xin-Yi Xia; Yang Zhou; Lin Gao; Xue-Jun Shang; Tong Ni; Wei-Ping Wang; Xiao-Buo Fan; Hong-Lin Yin; Shao-Jun Jiang; Bing Yao; Yu-An Hu; Gang Wang; Xiao-Jun Li
Journal:  PLoS One       Date:  2013-11-05       Impact factor: 3.240
  3 in total

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