MMRL invites participation and collaboration in research projects particularly in individuals, or preferably, large families with any of the following: Brugada Syndrome, Spontaneous Brugada ECG phenotype, Brugada phenotype unmasked or induced by sodium channel blockers,  Familial Atrial Fibrillation, Catecholamine-sensitive VT, Non-ischemia-related VT/VF occurring in young individuals, Post-MI QT prolongation and Torsade de Pointes,  Progressive Conduction Disease, Sudden death in infants and children (including SIDS), Acquired Long QT Syndrome and Short QT Syndrome.

For more information on participating in research call toll-free 1-888-888-MMRL or visit their website at:
http://www.mmrl.edu/