Carregant...
Sudden Infant Death Syndrome in Mice with an Inherited Mutation in RyR2
BACKGROUND: Mutations in the cardiac ryanodine receptor gene (RYR2) have been recently identified in victims of sudden infant death syndrome (SIDS). The aim of this study was to determine whether a gain-of-function mutation in RYR2 increases the propensity to cardiac arrhythmias and sudden death in...
Guardat en:
| Autors principals: | , , , , , , , , , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2796595/ https://ncbi.nlm.nih.gov/pubmed/20009080 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCEP.109.894683 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|