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Article

Identification of a novel ADAR mutation in a Chinese family with dyschromatosis symmetrica hereditaria (DSH).

Archives of dermatological research - 1 Sept 2005

Xing Qinghe, Wang Mingtai, Chen Xiangdong, Qian Xueqing, Qin Wei, Gao Jianjun, Wu Shengnan, Gao Rui, Feng Guoyin, He Lin

Abstract excerpt

Dyschromatosis symmetrica hereditaria (DSH [MIM 127400]) is characterized by the presence of hyperpigmented and hypopigmented macules mostly on the dorsal aspects of the extremities. Genetic studies have identified mutations in the ADAR gene, encoding double-stranded RNA-specific adenosine deamin...

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Source

Identifiers

PMID: 16133458
DOI: 10.1007/s00403-005-0589-1

Genes

ADAR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16133458-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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