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Article

Genetic basis of hypertrophic cardiomyopathy in children.

Clinical research in cardiology : official journal of the German Cardiac Society - 1 Mar 2019

Rupp Stefan, Felimban Moataz, Schänzer Anne, Schranz Dietmar, Marschall Christoph, Zenker Martin, Logeswaran Thushiha, Neuhäuser Christoph, Thul Josef, Jux Christian, Hahn Andreas

Abstract excerpt

BACKGROUND: Previous investigations assessing the genetic cause of pediatric hypertrophic cardiomyopathy (HCM) found underlying genetic mutations in 50-60% of cases. The purpose of our study was to analyze whether this number can be augmented by applying next-generation sequencing and directing further diagnostics by discussing unsolved cases in a multidisciplinary board. METHODS AND RESULTS: 42 patients with the...

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Share to Adaptor Proteins, Signal Transducing
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiomyopathy, Hypertrophic

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Share to High-Throughput Nucleotide Sequencing

Share to Infant, Newborn

Source

Identifiers

PMID: 30105547
DOI: 10.1007/s00392-018-1354-8

Genes

BAG3
GAA
LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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