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

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

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Citations

41

References

1994

Year

Ludwig Thierfelder, Hugh Watkins, Calum A. MacRae, Roger Lamas, William J. McKenna, Hans-Peter Vosberg, J.G. Seldman, Christine E. Seidman

Cardiac MuscleCardiomyopathyFamilial Hypertrophic CardiomyopathyPathologyMedicineCardiologyCardiovascular GeneticsCardiac Pathology

References

	Year	Citations

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