Concepedia

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

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

Cell · 1994 · 1K citations · 41 references

DOI

Concepts

References

41

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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Exon definition may facilitate splice site selection in RNAs with multiple exons.

Barbara Robberson, Gilbert J. Cote, Susan M. Berget · Molecular and Cellular Biology · 1990 · 712 citations · Full text

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Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1

John A. Jarcho, William J. McKenna, Jean-Pierre Pare et al. · New England Journal of Medicine · 1989 · 540 citations

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Troponin T isoform expression in humans. A comparison among normal and failing adult heart, fetal heart, and adult and fetal skeletal muscle.

Page A.W. Anderson, Nadia N. Malouf, Annette E. Oakeley et al. · Circulation Research · 1991 · 380 citations

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Hypertrophic Cardiomyopathy

Barry J. Maron, Robert O. Bonow, Richard O. Cannon et al. · New England Journal of Medicine · 1987 · 378 citations

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