Myocardial perfusion and sympathetic innervation in patients with hypertrophic cardiomyopathy

α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

Ludwig Thierfelder, Hugh Watkins, Calum A. MacRae et al. · Cell · 1994 · 1K citations

Medicine, Genetics, Molecular Genetics +10

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

Karl Poetter, He Jiang, Shahin Hassanzadeh et al. · Nature Genetics · 1996 · 585 citations

Medicine, Genetics, Molecular Genetics +16

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

Akinori Kimura, Haruhito Harada, Jeong-Euy Park et al. · Nature Genetics · 1997 · 577 citations

Medicine, Genetics, Molecular Genetics +12

Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

Gisèle Bonne, Lucie Carrier, J. Bercovici et al. · Nature Genetics · 1995 · 443 citations

Medicine, Genetics, Molecular Genetics +9

Coronary vasodilation is impaired in both hypertrophied and nonhypertrophied myocardium of patients with hypertrophic cardiomyopathy: A study with nitrogen-13 ammonia and positron emission tomography

P.G. Camici, Giampaolo Chiriatti, Roberto Lorenzoni et al. · Journal of the American College of Cardiology · 1991 · 338 citations

Medicine, Cardiology, Physiology +13