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Calsequestrin Mutation and Catecholaminergic Polymorphic Ventricular Tachycardia: A Simulation Study of Cellular Mechanism
OBJECTIVES: Patients with a missense mutation of the calsequestrin 2 gene (CASQ2) are at risk for catecholaminergic polymorphic ventricular tachycardia. This mutation (CASQ2 (D307H)) results in decreased ability of CASQ2 to bind Ca(2+) in the sarcoplasmic reticulum (SR). In this theoretical study, w...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2007
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2030636/ https://ncbi.nlm.nih.gov/pubmed/17531962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cardiores.2007.04.010 |
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