Detalhe da pesquisa
1.
Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome.
Am J Med Genet A
; 185(11): 3433-3445, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34415104
2.
Genetic homozygosity in a diverse population: An experience of long QT syndrome.
Int J Cardiol
; 316: 117-124, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32470535