| 1 | PCCD2, SCN5A
|
| Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.
|
| Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA.
|
| Hum Mol Genet 11(3):337-45. 2002
|
| 2 | PCCD2, SCN5A
|
| Novel mutations in domain I of SCN5A cause Brugada syndrome.
|
| Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA.
|
| Mol Genet Metab 75(4):317-24. 2002
|
| 3 | SCN5A, PCCD2
|
| Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation.
|
| Grant AO, Carboni MP, Neplioueva V, Starmer CF, Memmi M, Napolitano C, Priori S.
|
| J Clin Invest 110(8):1201-9. 2002
|
| 4 | PCCD1, PCCD2, SCN5A
|
| A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome.
|
| Akai J, Makita N, Sakurada H, Shirai N, Ueda K, Kitabatake A, Nakazawa K, Kimura A, Hiraoka M.
|
| FEBS Lett 479(1-2):29-34. 2000
|
| 5 | PCCD2, SCN5A, BRGS1
|
| Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.
|
| Rook MB, Alshinawi CB, Groenewegen WA, van Gelder IC, van Ginneken AC, Jongsma HJ, Mannens MM, Wilde AA.
|
| Cardiovasc Res 44(3):507-17. 1999
|
| 6 | PCCD2, SCN5A
|
| Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.
|
| Chen Q, et al.
|
| Nature 392 : 293-295. 1998
|
| 7 | PCCD2
|
| Familial cardiomyopathy underlies syndrome of right bundle branch block, ST segment elevation and sudden death.
|
| Corrado D, et al.
|
| J Am Coll Cardiol 27 : 443-448. 1996
|
| 8 | PCCD2
|
| Right bundle branch block, persistent ST segment elevation and sudden cardiac death : a distinct clinical and electrocardiographic syndrome. A multicenter report.
|
| Brugada P, et al.
|
| J Am Coll Cardiol 20 : 1391-1396. 1992
|