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Article

[A familial form of conduction defects associated with a PRKAG2 gene mutation].

Archives des maladies du coeur et des vaisseaux - 1 Sept 2007

Pochmalicki G, Genest M, Richard P, Komajda M, Charron P

Abstract excerpt

Conduction defects are usually secondary to elective aging of the conduction pathways. However, some familial and genetic forms are now being described. Here we report a particular electrocardiographic pattern in four members of the same family over three generations, naturally leading to the sus...

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Source

Identifiers

PMID: 18033003

Genes

PRKAG2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18033003-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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