ロード中...
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...
保存先:
| 主要な著者: | , , , , , , , , , , , , , , , |
|---|---|
| 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 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|