Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

Brugada syndrome is a genetic disease associated with sudden cardiac death that is characterized by ventricular fibrillation and right precordial ST segment elevation on ECG. Loss-of-function mutations in SCN5A, which encodes the predominant cardiac sodium channel α subunit Na(V)1.5, can cause Bruga...

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Detalhes bibliográficos
Main Authors: Watanabe, Hiroshi, Koopmann, Tamara T., Le Scouarnec, Solena, Yang, Tao, Ingram, Christiana R., Schott, Jean-Jacques, Demolombe, Sophie, Probst, Vincent, Anselme, Frédéric, Escande, Denis, Wiesfeld, Ans C.P., Pfeufer, Arne, Kääb, Stefan, Wichmann, H.-Erich, Hasdemir, Can, Aizawa, Yoshifusa, Wilde, Arthur A.M., Roden, Dan M., Bezzina, Connie R.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2008
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2373423/
https://ncbi.nlm.nih.gov/pubmed/18464934
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI33891
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