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Article

Association of MTHFR A1298C polymorphism with conotruncal heart disease.

Cardiology in the young - 1 Oct 2015

Sayin Kocakap Beyza D, Sanli Cihat, Cabuk Feryal, Koc Murat, Kutsal Ali

Abstract excerpt

Congenital heart diseases are common congenital anomalies with 1% prevalence worldwide and are associated with significant childhood morbidity and mortality. Among a wide range of aetiologically heterogeneous conditions, conotruncal anomalies account for approximately one-third of all congenital...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25547204
DOI: 10.1017/S1047951114002467

Genes

MTHFR
NNMT

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25547204-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Association of MTHFR A1298C polymorphism with conotruncal heart disease.PMID 25547204Read ↗

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Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects.Semantic proximity Read ↗

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