Detalhe da pesquisa
1.
Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1.
J Cardiovasc Electrophysiol
; 33(2): 262-273, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34860437