ロード中...
Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutation()
BACKGROUND: Phenotypes often differ even within family members carrying the same SCN5A mutation. We aimed to evaluate the genetic modifiers in a family with Brugada syndrome (BrS) and sick sinus syndrome (SSS) with an SCN5A mutation that causes the truncated alpha-subunit of cardiac Na channel prote...
保存先:
| 出版年: | J Arrhythm |
|---|---|
| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Elsevier
2017
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5300865/ https://ncbi.nlm.nih.gov/pubmed/28217227 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joa.2016.05.007 |
| 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!
|