Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia

BACKGROUND: RYR2, encoding cardiac ryanodine receptor, is the major responsible gene for catecholaminergic polymorphic ventricular tachycardia (CPVT). Meanwhile, KCNJ2, encoding inward‐rectifier potassium channel (I(K1)), can be the responsible gene for atypical CPVT. We recently encountered a famil...

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Detalhes bibliográficos
Publicado no:Ann Noninvasive Electrocardiol
Main Authors: Dharmawan, Tommy, Nakajima, Tadashi, Ohno, Seiko, Iizuka, Takashi, Tamura, Shuntaro, Kaneko, Yoshiaki, Horie, Minoru, Kurabayashi, Masahiko
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6850420/
https://ncbi.nlm.nih.gov/pubmed/30615235
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12623
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