A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutationAnja A. T. Geisterfer-Lowrance, J G Seidman, Susan Kass et al.|Cell|1990Cited by 1.4k
α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomereLudwig Thierfelder, Christine E. Seidman, Calum A. MacRae et al.|Cell|1994Cited by 1k
A molecular basis for familial hypertrophic cardiomyopathy: An αβ cardiac myosin heavy chain hybrid geneG Tanigawa, Christine E. Seidman, John A. Jarcho et al.|Cell|1990Cited by 223
Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin GeneDomenico Coviello, Christine E. Seidman, Jonathan G. Seidman et al.|Journal of the American College of Cardiology|1997Cited by 127