Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities
2000 ◽
Vol 23
(3)
◽
pp. 407-409
◽
2001 ◽
Vol 24
(1)
◽
pp. 112-115
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2008 ◽
Vol 9
(8)
◽
pp. 842-846
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2018 ◽
Vol 71
(5)
◽
pp. 403-406