Article
The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria.
Journal of molecular medicine (Berlin, Germany) - 1 Mar 2023
Chen Hongyu, Yang Pingping, Yang Dan, Wang Dongsheng, Lu Mao, Li Yadong, Zhong Zhiqiang, Zhang Jing, Zeng Zhen, Liu Zhi, Zeng Xiaohua, Jia Xu, Xing Qinghe, Zhou Ding'an
Abstract excerpt
Dyschromatosis universalis hereditaria (DUH) is a pigmentary genodermatosis characterized by a mixture of hyperpigmented and hypopigmented macules distributed randomly over the body. Although Sterile Alpha motif- and SH3 domain-containing protein 1 (SASH1) and ATP-binding cassette subfamily B, member 6 (ABCB6) have been identified as causative genes for this disorder, some cases involve unknown pathogenic genes....
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