Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Pathogenicity of ADAR1 mutation in a Chinese family with dyschromatosis symmetrica hereditaria.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Nov 2017

Zhang S-D, Feng S-J, Nh-Tseung K, Zhao J-J

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenosine Deaminase
Share to Asian People
Share to China
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Pigmentation Disorders

Share to RNA-Binding Proteins

Source

Identifiers

PMID: 28502085
DOI: 10.1111/jdv.14331

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pathogenicity of ADAR1 mutation in a Chinese family with dyschromatosis symmetrica hereditaria.PMID 28502085Read ↗

Two novel splice site mutations of the ADAR1 gene in Chinese families with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

Genetic spectrum of dyschromatosis symmetrica hereditaria in Chinese patients including a novel nonstop mutation in ADAR1 gene.Semantic proximity Read ↗

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

A novel missense mutation of ADAR1 gene in a Chinese family leading to dyschromatosis symmetrica hereditaria and literature review.Semantic proximity Read ↗

Eight Novel Mutations of the ADAR1 Gene in Chinese Patients with Dyschromatosis Symmetrica Hereditaria.Semantic proximity Read ↗

Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations.Semantic proximity Read ↗

Novel de novo heterozygous frameshift mutation of the ADAR1 gene in heavy dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

Identification of a novel mutation in the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

Mutations in the ADAR1 gene in Chinese families with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patient.Semantic proximity Read ↗

Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

[Analysis of a Chinese pedigree affected with dyschromatosis symmetrica hereditaria due to a novel variant of ADAR gene].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.