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Article

Familial atrial septal defect in the oval fossa with progressive prolongation of the atrioventricular conduction caused by mutations in the NKX2.5 gene.

Cardiology in the young - 1 Feb 2009

Bjørnstad Per G, Leren Trond P

Abstract excerpt

OBJECTIVE: To search for a genetic basis in a family with autosomal dominantly inherited atrial septal defect in combination with increasing conduction anomalies. DESIGN: We searched for mutations in the NKX2.5 gene by sequencing of desoxyribonucleic acid in a previously investigated family. PATIENTS: All family members were included if they, after informed consent, had decided to participate in the genetic...

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Share to Chromosomes, Human, Pair 5
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Septal Defects, Atrial

Share to Homeobox Protein Nkx-2.5

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Source

Identifiers

PMID: 19049681
DOI: 10.1017/S1047951108003387

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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