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Heterogeneity of Ryanodine Receptor Dysfunction in a Mouse Model Of Catecholaminergic Polymorphic Ventricular Tachycardia
RATIONALE: Most cardiac ryanodine receptor (RyR2) mutations associated with Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) are postulated to cause one distinctive form of Ca(2+) release dysfunction. Considering the spread distribution of CPVT mutations, we hypothesized that dysfunction...
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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2012
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3549355/ https://ncbi.nlm.nih.gov/pubmed/23152493 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCRESAHA.112.274803 |
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