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

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

Dermatology (Basel, Switzerland) - 1 Jan 2006

Liu Yan, Xiao Shengxiang, Peng Zhenhui, Chu Yonglie, Wang Junmin, Li Xiaoli, Zhou Shaona

Abstract excerpt

BACKGROUND: Dyschromatosis symmetrica hereditaria (DSH) is a pigmentary genodermatosis characterized by a mixture of hyperpigmented and hypopigmented macules localized on the back of the extremities and caused by mutations in the double-stranded RNA-specific adenosine deaminase (DSRAD) gene. OBJE...

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 China
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Mutation, Missense

Share to Pigmentation

Share to Pigmentation Disorders

Share to RNA-Binding Proteins

Source

Identifiers

PMID: 17033168
DOI: 10.1159/000095036

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17033168-2026-09-02.2. 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

A new mutation of the double-stranded RNA-specific adenosine deaminase gene in a family with dyschromatosis symmetrica hereditaria.PMID 17033168Read ↗

Identification of a novel DSRAD gene mutation in a Chinese family 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 ↗

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

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in 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 ↗

Two frameshift mutations in the RNA-specific adenosine deaminase gene associated with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

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

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

Five novel mutations of RNA-specific adenosine deaminase gene 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 ↗

Identification of Five Novel Variants of ADAR1 in Dyschromatosis Symmetrica Hereditaria by Next-generation SequencingSemantic proximity Read ↗

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