Detalhe da pesquisa
1.
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Hum Mol Genet;
24(10): 2757-63, 2015 May 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25650408
2.
Dysfunction of the Voltage-Gated K+ Channel ß2 Subunit in a Familial Case of Brugada Syndrome.
J Am Heart Assoc;
5(6)2016 06 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27287695