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 NPPA variants associated with atrial fibrillation in a Chinese GeneID population.

Clinica chimica acta; international journal of clinical chemistry - 2 Apr 2010

Ren Xiang, Xu Chengqi, Zhan Chengxiong, Yang Yanzong, Shi Lisong, Wang Fan, Wang Chuchu, Xia Yunlong, Yang Bo, Wu Gang, Wang Pengyun, Li Xiuchun, Wang Dan, Xiong Xin, Liu Jinqiu, Liu Ying, Liu Mugen, Liu Jingyu, Tu Xin, Wang Qing Kenneth

Abstract excerpt

BACKGROUND: A frameshift mutation in the NPPA gene was identified in 1 family with atrial fibrillation (AF), however, further studies are needed to establish unequivocally the genetic association between NPPA and AF. METHODS: A case control association study and mutational analysis of NPPA were p...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Atrial Fibrillation

Share to Atrial Natriuretic Factor

Share to Genetic Variation

Share to Mutation

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 20064500
DOI: 10.1016/j.cca.2009.12.019

Genes

NPPA

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20064500-2026-09-02.2. 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 NPPA variants associated with atrial fibrillation in a Chinese GeneID population.PMID 20064500Read ↗

Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation.Semantic proximity Read ↗

Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation.Semantic proximity Read ↗

A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation.Semantic proximity Read ↗

Genetic aspects of lone atrial fibrillation: what do we know?Semantic proximity Read ↗

Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.Semantic proximity Read ↗

Common variants in KCNN3 are associated with lone atrial fibrillation.Semantic proximity Read ↗

Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population.Semantic proximity Read ↗

Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation.Semantic proximity Read ↗

Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases.Semantic proximity Read ↗

Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population.Semantic proximity Read ↗

Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population.Semantic proximity Read ↗

Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years.Semantic proximity Read ↗

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