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Article

Absence of GJA1 gene mutations in four patients with anomalous left coronary artery from the pulmonary artery (ALCAPA).

Le Journal medical libanais. The Lebanese medical journal - 1 Jan 2000

Sawaya Fadi, Souki Ramzi, Arabi Mariam, Majdalani Marianne, Obeid Mounir, Bitar Fadi F, Nemer Georges

Abstract excerpt

PROBLEM: Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare form of congenital heart disease with no known genetic cause. It is usually diagnosed within the first year of life; it results in myocardial cell death, congestive heart failure and lethality if left untreated. Connexin 43alpha1 is a member of the gap junction family of proteins demonstrated by animal studies to have a role in...

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Identifiers

PMID: 22259903

Genes

GJA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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