Whole gene sequencing identifies deep-intronic variants with potential functional impact in patients with hypertrophic cardiomyopathy

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Application of Genetic Testing in Hypertrophic Cardiomyopathy for Preclinical Disease Detection

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Significance of Sarcomere Gene Mutations Analysis in the End-Stage Phase of Hypertrophic Cardiomyopathy

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A systematic review and meta-analysis of genotype–phenotype associations in patients with hypertrophic cardiomyopathy caused by sarcomeric protein mutations

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Cardiac Titin and Heart Disease

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Mutations in NEXN, a Z-Disc Gene, Are Associated with Hypertrophic Cardiomyopathy

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Cardiac Ankyrin Repeat Protein Gene (ANKRD1) Mutations in Hypertrophic Cardiomyopathy

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Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

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