Embryonic type Na(+) channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome

SCN5A is abundant in heart and has a major role in I(Na). Loss-of-function mutation in SCN5A results in Brugada syndrome (BrS), which causes sudden death in adults. It remains unclear why disease phenotype does not manifest in the young even though mutated SCN5A is expressed in the young. The aim of...

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Detalles Bibliográficos
Autores principales: Okata, Shinichiro, Yuasa, Shinsuke, Suzuki, Tomoyuki, Ito, Shogo, Makita, Naomasa, Yoshida, Tetsu, Li, Min, Kurokawa, Junko, Seki, Tomohisa, Egashira, Toru, Aizawa, Yoshiyasu, Kodaira, Masaki, Motoda, Chikaaki, Yozu, Gakuto, Shimojima, Masaya, Hayashiji, Nozomi, Hashimoto, Hisayuki, Kuroda, Yusuke, Tanaka, Atsushi, Murata, Mitsushige, Aiba, Takeshi, Shimizu, Wataru, Horie, Minoru, Kamiya, Kaichiro, Furukawa, Tetsushi, Fukuda, Keiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039759/
https://www.ncbi.nlm.nih.gov/pubmed/27677334
http://dx.doi.org/10.1038/srep34198

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039759/
https://www.ncbi.nlm.nih.gov/pubmed/27677334
http://dx.doi.org/10.1038/srep34198

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