Concepedia

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

Gisèle Bonne, Lucie Carrier, J. Bercovici, Corinne Cruaud, Pascale Richard, Bernard Hainque, Mathias Gautel, Siegfried Labeit, Michael R. James, J. Beckmann,

Nature Genetics · 1995 · 443 citations · 26 references

DOI

Concepts

References

26

‘Touchdown’ PCR to circumvent spurious priming during gene amplification

R.H. Don, Peter Cox, Brandon J. Wainwright et al. · Nucleic Acids Research · 1991 · 2.6K citations · Full text

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A second-generation linkage map of the human genome

Jean Weissenbach, Gàbor Gyapay, Colette Dib et al. · Nature · 1992 · 1.7K citations

, , +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

, , +10

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

, , +10

Passive tension in cardiac muscle: contribution of collagen, titin, microtubules, and intermediate filaments

Henk L. Granzier, Thomas C. Irving · Biophysical Journal · 1995 · 643 citations · Full text

, , +16