Novel Calmodulin (CALM2) Mutations Associated with Congenital Arrhythmia Susceptibility

BACKGROUND: Genetic predisposition to life-threatening cardiac arrhythmias such as in congenital long-QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT) represent treatable causes of sudden cardiac death in young adults and children. Recently, mutations in calmodulin...

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Main Authors: Makita, Naomasa, Yagihara, Nobue, Crotti, Lia, Johnson, Christopher N., Beckmann, Britt-Maria, Roh, Michelle S., Shigemizu, Daichi, Lichtner, Peter, Ishikawa, Taisuke, Aiba, Takeshi, Homfray, Tessa, Behr, Elijah R., Klug, Didier, Denjoy, Isabelle, Mastantuono, Elisa, Theisen, Daniel, Tsunoda, Tatsuhiko, Satake, Wataru, Toda, Tatsushi, Nakagawa, Hidewaki, Tsuji, Yukiomi, Tsuchiya, Takeshi, Yamamoto, Hirokazu, Miyamoto, Yoshihiro, Endo, Naoto, Kimura, Akinori, Ozaki, Kouichi, Motomura, Hideki, Suda, Kenji, Tanaka, Toshihiro, Schwartz, Peter J., Meitinger, Thomas, Kääb, Stefan, Guicheney, Pascale, Shimizu, Wataru, Bhuiyan, Zahurul A., Watanabe, Hiroshi, Chazin, Walter J., George, Alfred L.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4140998/
https://ncbi.nlm.nih.gov/pubmed/24917665
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.113.000459
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