Lataa...
A novel KCNA5 Mutation Implicates Tyrosine Kinase Signaling in Human Atrial Fibrillation
BACKGROUND: Emerging evidence has strongly implicated hereditary determinants for atrial fibrillation (AF). Loss-of-function mutations in KCNA5 encoding the ultra-rapid delayed rectifier potassium current (I(Kur)) have been identified in AF families. OBJECTIVE: Our study sought to present the clinic...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2010
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2932792/ https://ncbi.nlm.nih.gov/pubmed/20638934 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2010.05.032 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|