TY - JOUR
T1 - Familial hypertrophic cardiomyopathy: Functional effects of myosin mutation R723G in cardiomyocytes
AU - Kraft, T.
AU - Witjas-Paalberends, E.R.
AU - Boontje, N.
AU - Tripathi, S.
AU - Brandis, A.
AU - Montag, J.
AU - Hodgkinson, J.L.
AU - Francino, A.
AU - Navarro-Lopez, F.
AU - Brenner, B.
AU - Stienen, G.J.M.
AU - van der Velden, J.
PY - 2013
Y1 - 2013
N2 - Familial Hypertrophic Cardiomyopathy (FHC) is frequently caused by mutations in the β-cardiac myosin heavy chain (β-MyHC). To identify changes in sarcomeric function triggered by such mutations, distinguishing mutation effects from other functional alterations of the myocardium is essential. We previously identified a direct effect of mutation R723G (MyHC
AB - Familial Hypertrophic Cardiomyopathy (FHC) is frequently caused by mutations in the β-cardiac myosin heavy chain (β-MyHC). To identify changes in sarcomeric function triggered by such mutations, distinguishing mutation effects from other functional alterations of the myocardium is essential. We previously identified a direct effect of mutation R723G (MyHC
UR - https://www.scopus.com/pages/publications/84875271449
UR - https://www.scopus.com/inward/citedby.url?scp=84875271449&partnerID=8YFLogxK
U2 - 10.1016/j.yjmcc.2013.01.001
DO - 10.1016/j.yjmcc.2013.01.001
M3 - Article
SN - 0022-2828
VL - 57
SP - 13
EP - 22
JO - Journal of Molecular and Cellular Cardiology
JF - Journal of Molecular and Cellular Cardiology
ER -
