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
Inglês
| MEDLINE | ID: mdl-25650408
2.
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.
J Am Coll Cardiol
; 70(3): 358-370, 2017 Jul 18.
Artigo
Inglês
| MEDLINE | ID: mdl-28705318
3.
Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block.
J Am Heart Assoc
; 5(5)2016 05 20.
Artigo
Inglês
| MEDLINE | ID: mdl-27207958
4.
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I.
Int J Cardiol
; 207: 349-58, 2016 Mar 15.
Artigo
Inglês
| MEDLINE | ID: mdl-26820365