ARG92GLN mutation in cTnT linked to familial hypertrophic cardiomyopathy causes increased Ca2+ sensitivity in mouse cardiac myofilaments. Journal Article uri icon

Overview

publication date

  • January 1, 1999

Full Author List

  • Chandra M; McManus-Rundell V; Tardiff J; Leinwand LA; de Tombe P; Solaro RJ

Additional Document Info

start page

  • A278

end page

  • A278

volume

  • 76

issue

  • 1