α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
Ludwig Thierfelder(Amsterdam UMC Location University of Amsterdam), Christine E. Seidman(Harvard University), Hugh Watkins(John Radcliffe Hospital), J.G. Seldman(Howard Hughes Medical Institute), Calum A. MacRae(Brigham and Women's Hospital), Roger Lamas(Hospital Militar de Santiago), Hans-Peter Vosberg(Max Planck Institute for Medical Research), William J. McKenna(British Heart Foundation)
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