kw.\*:("Inherited arrhythmias")
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Genetics of sudden death: focus on inherited channelopathiesCERRONE, Marina; PRIORI, Silvia G.European heart journal. 2011, Vol 32, Num 17, pp 2109-2118, issn 0195-668X, 10 p.Article
Familial clustering of lone atrial fibrillation in patients with saddleback-type ST-segment elevation in right precordial leadsJUHANI JUNTTILA, M; PEKKA RAATIKAINEN, M. J; PERKJÖMÄKI, Juha S et al.European heart journal. 2007, Vol 28, Num 4, pp 463-468, issn 0195-668X, 6 p.Article
A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardiaTAN, Bi-Hua; ITURRALDE-TORRES, Pedro; MEDEIROS-DOMINGO, Argelia et al.Cardiovascular research. 2007, Vol 76, Num 3, pp 409-417, issn 0008-6363, 9 p.Article
Loss-of-function mutation of the SCN3B-encoded sodium channel β3 subunit associated with a case of idiopathic ventricular fibrillationVALDIVIA, Carmen R; MEDEIROS-DOMINGO, Argelia; BIN YE et al.Cardiovascular research. 2010, Vol 86, Num 3, pp 392-400, issn 0008-6363, 9 p.Article