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The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance

The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_4a0eab178ea2475f8cb5771fda522b81

The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance

About this item

Full title

The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance

Publisher

England: BioMed Central Ltd

Journal title

Journal of cardiovascular magnetic resonance, 2012-02, Vol.14 (1), p.17-17, Article 12

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Hypertrophic cardiomyopathy (HCM) is the most common genetic disease of the heart. HCM is characterized by a wide range of clinical expression, ranging from asymptomatic mutation carriers to sudden cardiac death as the first manifestation of the disease. Over 1000 mutations have been identified, classically in genes encoding sarcomeric proteins. No...

Alternative Titles

Full title

The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_4a0eab178ea2475f8cb5771fda522b81

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_4a0eab178ea2475f8cb5771fda522b81

Other Identifiers

ISSN

1097-6647,1532-429X

E-ISSN

1532-429X

DOI

10.1186/1532-429X-14-17

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