Wordt geladen...
Short QT syndrome Genotype-phenotype correlations
The short QT syndrome is a new congenital entity associated with familial atrial fibrillation and/or sudden death or syncope. Three different gain-of-function mutations in genes encoding for cardiac potassium channels (KCNH2, KCNQ1, and KCNJ2) have been identified up to now to cause short QT syndrom...
Bewaard in:
| Hoofdauteurs: | , , , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2005
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1474068/ https://ncbi.nlm.nih.gov/pubmed/16226079 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jelectrocard.2005.06.009 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|