Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy

Hypertrophic Cardiomyopathy

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Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

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Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

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Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy

Iacopo Olivotto, Francesca Girolami, Michael J. Ackerman et al. · Mayo Clinic Proceedings · 2008 · 325 citations

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