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Article

Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria.

Archives of dermatological research - 1 Aug 2010

Li Ming, Yang Lijia, Li Chengrang, Jin Cheng, Lai Meiling, Zhang Guolong, Hu Yan, Ji Jin, Yao Zhirong

Abstract excerpt

Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant cutaneous disorder characterized by a mixture of hyperpigmented and hypopigmented macules of various sizes on the extremities and caused by the mutations of adenosine deaminase acting on RNA1 (ADAR1) gene. We screened 14 unr...

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PMID: 20186421
DOI: 10.1007/s00403-010-1039-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20186421-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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