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Article

Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.

Cardiology in the young - 1 Jun 2007

Selamet Tierney Elif Seda, Marans Zvi, Rutkin Melissa B, Chung Wendy K

Abstract excerpt

OBJECTIVES: This study was designed to assess the frequency and types of genetic variants in CFC1 in children with laterality disorders associated with cardiovascular involvement. BACKGROUND: Laterality syndromes are estimated to comprise 3% of neonates with congenital cardiac disease. Genetic pr...

Read the complete abstract on PubMed

Topics

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Share to Body Patterning
Share to Gene Expression Regulation, Developmental
Share to Gene Frequency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Defects, Congenital

Share to Intercellular Signaling Peptides and Proteins

Share to Mutation, Missense

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 17445335
DOI: 10.1017/S1047951107000455

Genes

CFC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17445335-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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