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

Identification of two novel DSRAD mutations in two Chinese families with dyschromatosis symmetrica hereditaria.

Archives of dermatological research - 1 Dec 2006

Lu Jianyun, Liao Zhaohui, Chen Jing, Xiang Yaping, Wu Zhiqiang, Zuo Chengxin, Jiang Xianzhen, Huang Jinhua

Abstract excerpt

Dyschromatosis symmetrica hereditaria (DSH) is a hereditary skin disease characterized by the presence of hyperpigmented and hypopigmented macules on face and dorsal aspects of the extremities that appear in infancy or early childhood. Genetic studies have identified mutations in the double-stran...

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 Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

Share to Pedigree

Share to Pigmentation Disorders

Share to RNA, Double-Stranded

Source

Identifiers

PMID: 17021765
DOI: 10.1007/s00403-006-0701-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17021765-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of two novel DSRAD mutations in two Chinese families with dyschromatosis symmetrica hereditaria.PMID 17021765Read ↗

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

Identification of two novel mutations in Chinese patients with Dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

A new mutation of the double-stranded RNA-specific adenosine deaminase gene in a family with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

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

A new arginine substitution mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH).Semantic proximity Read ↗

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

Four novel mutations of ADAR1 in Chinese patients with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

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

A novel insertion mutation in the ADAR1 gene of a Chinese family with 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 ↗

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