R. Malti

A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field

J. Lusson, P. Acar, J. Roume, 2015, European Journal of Human Genetics.

Evidence for genetic heterogeneity in Carvajal syndrome

P. Bouvagnet, N. Roux-Buisson, N. Nehme, 2012, Cell and Tissue Research.

A human MYBPC3 mutation appearing about 10 centuries ago results in a hypertrophic cardiomyopathy with delayed onset, moderate evolution but with a risk of sudden death

F. Fellmann, X. André-Fouët, G. Millat, 2012, BMC Medical Genetics.

Evidence for genetic heterogeneity in Carvajal syndrome

P. Bouvagnet, N. Roux-Buisson, N. Nehme, 2012, Cell and Tissue Research.