dx.doi.org/10.1038/ejhg.2014.211, hdl.handle.net/1765/85935
European Journal of Human Genetics
Department of Cardiology

Wessels, M.W, Herkert, J.C, Frohn-Mulder, I.M.E, Dalinghaus, M, van den Wijngaard, A, de Krijger, R.R, … Dooijes, D. (2015). Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects. European Journal of Human Genetics, 23(7), 922–928. doi:10.1038/ejhg.2014.211