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Article

Clinical features, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy in South Africans.

Cardiovascular journal of Africa - 1 Jan 2000

Ntusi Ntobeko A, Shaboodien Gasnat, Badri Motasim, Gumedze Freedom, Mayosi Bongani M

Abstract excerpt

BACKGROUND: Little is known about the clinical characteristics, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy (HCM) in Africans. The objective of this study was to delineate the clinical and genetic features and outcome of HCM in African patients. METHODS: Information on clinical presentation, electrocardiographic and echocardiographic findings, and outcome of cases with HCM was...

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Topics

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Share to Cardiac Myosins
Share to Cardiomyopathy, Hypertrophic, Familial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 27841901
DOI: 10.5830/CVJA-2015-075
PMCID: PMC5101433

Genes

MYH7
MYBPC3
ACTC1
CSRP3
FHL1
GLA
LAMP2
LMNA
MYL2
MYL3
PLN
PRKAG2
TNNI3
TNNT2
TPM1

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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