Concepedia

Clinical manifestations of hypertrophiccardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene

Yoshinori Koga, Hironori Toshima, Akinori Kimura, Haruhito Harada, Takeshi Koyanagi, Hirofumi Nishi, Masashi Nakata, Tsutomu Imaizumi

Journal of Cardiac Failure · 1996 · 28 citations · 14 references

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14

A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation

Anja A. T. Geisterfer-Lowrance, Susan Kass, G Tanigawa et al. · Cell · 1990 · 1.4K citations

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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

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Mutations in the Genes for Cardiac Troponin T and α-Tropomyosin in Hypertrophic Cardiomyopathy

Hugh Watkins, William J. McKenna, Ludwig Thierfelder et al. · New England Journal of Medicine · 1995 · 932 citations · Full text

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Characteristics and Prognostic Implications of Myosin Missense Mutations in Familial Hypertrophic Cardiomyopathy

Hugh Watkins, Anthony Rosenzweig, Dar‐San Hwang et al. · New England Journal of Medicine · 1992 · 746 citations · Full text

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Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

Hugh Watkins, David A. Conner, Ludwig Thierfelder et al. · Nature Genetics · 1995 · 589 citations

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