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

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

Dyschromatosis universalis hereditaria (DUH) is a rare heterogeneous pigmentary genodermatosis, which was first described in 1933. The genetic cause has recently been discovered by the discovery of mutations in ABCB6. Here we investigated a Chinese family with typical features of autosomal dominant...

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Bibliographic Details
Main 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
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3818219?pdf=render

Internet

http://europepmc.org/articles/PMC3818219?pdf=render

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