RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome
Belbachir, N., Portero, V., Gourraud, J.B., Jesel, L., Guilluy, C., Gaborit, N., Girardeau, A., Bonnaud, S., Pattier, S., Scott, C., Burel, S., Gaignerie, A., Genin, E., Deleuze, J.F., Dina, C., SchotVolume:
10
Language:
english
Journal:
Archives of Cardiovascular Diseases Supplements
DOI:
10.1016/j.acvdsp.2018.02.044
Date:
April, 2018
File:
PDF, 159 KB
english, 2018