Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
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London: Nature Publishing Group UK
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English
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London: Nature Publishing Group UK
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Contents
Hypertrophic cardiomyopathy (HCM) was traditionally described as an autosomal dominant Mendelian disease but is now increasingly recognized as having a complex genetic aetiology. Although eight core genes encoding sarcomeric proteins account for >90% of the pathogenic variants in patients with HCM, variants in several additional genes (
ACTN2
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Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
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TN_cdi_proquest_miscellaneous_2573436086
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2573436086
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ISSN
1759-5002
E-ISSN
1759-5010
DOI
10.1038/s41569-021-00608-2
