Clinical and molecular data define a diagnosis of arrhythmogenic cardiomyopathy in a carrier of a brugada-syndrome-associated PKP2 mutation

S. Persampieri, C.A. Pilato, E. Sommariva, A.S. Maione, I. Stadiotti, A. Ranalletta, M. Torchio, A. Dello Russo, C. Basso, G. Pompilio, C. Tondo, M. Casella

Research output: Contribution to journalArticlepeer-review

Cite this