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Frontiers | Novel compound heterozygous ALPK3 mutations (c.4234C>T and c.3491G>A), causing hypertrophic cardiomyopathy treated with the liwen procedure: case report
1 Introduction Hypertrophic cardiomyopathy(HCM) is the most common autosomal dominant cardiovascular disease, mainly due to a pathogenic variant of the gene encoding sarcomeric proteins, or a cardiomyopathy characterised by myocardial hypertrophy of unknown etiology, the need to exclude other cardiovascular diseases or systemic, metabolic diseases caused by ventricular wall thickening, echocardiography or magnetic resonance examination of the left ventricle at end-diastole in any part of the...
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