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Article

A novel splice site mutation in the ADAR gene leading to exon skipping and dyschromatosis symmetrica hereditaria in a Japanese patient.

Clinical and experimental dermatology - 1 Dec 2016

Ansai O, Shigehara Y, Ito A, Abe R, Shimomura Y

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Share to Adenosine Deaminase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27747905
DOI: 10.1111/ced.12981

Genes

ADAR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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