Mutations in the cardiac Ryanodine Receptor gene (RYR2) cause dominant catecholaminergic polymorphic ventricular tachycardia (CPVT), a leading cause of sudden death in apparently healthy individuals exposed to emotions or physical exercise.

Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2) / Bongianino, R., Denegri, M., Mazzanti, A., Lodola, F., Vollero, A., Boncompagni, S., Fasciano, S., Rizzo, G., Mangione, D., Barbaro, S., Di Fonso, A., Napolitano, C., Auricchio, A., Protasi, F., Priori, S.G.. - In: CIRCULATION RESEARCH. - ISSN 0009-7330. - 121:5(2017), pp. 525-536-536. [10.1161/CIRCRESAHA.117.310882]

Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2)

AURICCHIO, ALBERTO;
2017

Abstract

Mutations in the cardiac Ryanodine Receptor gene (RYR2) cause dominant catecholaminergic polymorphic ventricular tachycardia (CPVT), a leading cause of sudden death in apparently healthy individuals exposed to emotions or physical exercise.
2017
Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2) / Bongianino, R., Denegri, M., Mazzanti, A., Lodola, F., Vollero, A., Boncompagni, S., Fasciano, S., Rizzo, G., Mangione, D., Barbaro, S., Di Fonso, A., Napolitano, C., Auricchio, A., Protasi, F., Priori, S.G.. - In: CIRCULATION RESEARCH. - ISSN 0009-7330. - 121:5(2017), pp. 525-536-536. [10.1161/CIRCRESAHA.117.310882]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/682825
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