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α-1-Syntrophin Mutation and the Long-QT Syndrome: A Disease of Sodium Channel Disruption

BACKGROUND: Long-QT syndrome (LQTS) is an inherited disorder associated with sudden cardiac death. The cytoskeletal protein syntrophin-α(1) (SNTA1) is known to interact with the cardiac sodium channel (hNa(v)1.5), and we hypothesized that SNTA1 mutations might cause phenotypic LQTS in patients with...

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書誌詳細
主要な著者: Wu, Geru, Ai, Tomohiko, Kim, Jeffrey J., Mohapatra, Bhagyalaxmi, Xi, Yutao, Li, Zhaohui, Abbasi, Shahrzad, Purevjav, Enkhsaikhan, Samani, Kaveh, Ackerman, Michael J, Qi, Ming, Moss, Arthur J., Shimizu, Wataru, Towbin, Jeffrey A., Cheng, Jie, Vatta, Matteo
フォーマット: Artigo
言語:Inglês
出版事項: 2008
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2726717/
https://ncbi.nlm.nih.gov/pubmed/19684871
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCEP.108.769224
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