Matteo Vatta

Ionic Mechanisms Responsible for the Electrocardiographic Phenotype of the Brugada

J. Towbin, R. Dumaine, V. Nesterenko, 1999 .

Genetic basis of hypertrophic cardiomyopathy

J. Towbin, M. Vatta, Xiaolei Xu, 2010 .

Molecular biology and the prolonged QT syndromes.

J. Towbin, M. Vatta, J A Towbin, 2001, The American journal of medicine.

Genetics of brugada, long QT, and arrhythmogenic right ventricular dysplasia syndromes.

J. Towbin, M. Vatta, Hua Li, 2000, Journal of electrocardiology.

A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy.

L. Mestroni, M. Giacca, F. Muntoni, 1996, Human molecular genetics.