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Familial dilated cardiomyopathy (DCM) is characterized by ventricular dilation and depressed myocardial performance. It is a… Expand TIA1 mutations cause Welander distal myopathy. MYH7 mutations result in various clinical phenotypes, including Laing distal… Expand Here we report on a case of MYH7-related myopathy in a boy with early onset of muscular weakness and delayed motor development in… Expand BackgroundMyosin heavy chain 7 related myopathies are rare disorders characterized by a wide phenotypic spectrum and… Expand To search for genes associated with migratory phenotypes in songbirds, we selected candidate genes through annotations from the… Expand Mutations in the beta-myosin heavy chain gene (MYH7) cause different muscle disorders. The specific molecular pathobiological… Expand Laing early onset distal myopathy and myosin storage myopathy are caused by mutations of slow skeletal/β‐cardiac myosin heavy… Expand Left ventricular noncompaction (LVNC) is a relatively common genetic cardiomyopathy, characterized by prominent trabeculations… Expand INTRODUCTION AND OBJECTIVES
Mutation of a sarcomeric gene is the most frequent cause of hypertrophic cardiomyopathy. For each… Expand An unusual clinical history of a 23-year-old male proband with obstructive hypertrophic cardiomyopathy associated with a rare… Expand