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Article

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy.

Human molecular genetics - 1 Nov 2014

Theis Jeanne L, Zimmermann Michael T, Larsen Brandon T, Rybakova Inna N, Long Pamela A, Evans Jared M, Middha Sumit, de Andrade Mariza, Moss Richard L, Wieben Eric D, Michels Virginia V, Olson Timothy M

Abstract excerpt

Locus mapping has uncovered diverse etiologies for familial atrial fibrillation (AF), dilated cardiomyopathy (DCM), and mixed cardiac phenotype syndromes, yet the molecular basis for these disorders remains idiopathic in most cases. Whole-exome sequencing (WES) provides a powerful new tool for fa...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 24925317
DOI: 10.1093/hmg/ddu297
PMCID: PMC4189907

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24925317-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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