Monomorphic and Polymorphic Ventricular Arrhythmias in Heterozygous Calsequestrin-2 Mutation Carriers.

Juan Jiménez-Jáimez, Mercedes Cabrera Ramos, Francisco Bermúdez-Jiménez, José Manuel García Pinilla, Ainhoa Robles Mezcua, Rosa Macías Ruiz, Miguel Álvarez, Luis Tercedor

Journal: Circulation. Genomic and precision medicine 2022;15(2):e003518

PMID: 35119302

Full Text on Atypon View on PubMed

Abstract

Address: Cardiology Department, Hospital Universitario Virgen de las Nieves, Granada, Spain (J.J.-J., F.B.-J., R.M.R., M.A., L.T.).; Cardiology Department, Hospital Universitario lozano Blesa, Zaragoza, Spain (J.J.-J., F.B.-J., R.M.R., M.A., L.T.).; Instituto de Investigación Biosanitaria (ibs.GRANADA), Universidad de Granada, Spain (M.C.R.).; Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain (F.B.-J.).; Cardiology Department, Hospital Universitario Virgen de la Victoria, Málaga, Spain (J.M.G.P., A.R.M.).

DOI: 10.1161/CIRCGEN.121.003518

Link outs

Free resources

Medical:

https://medlineplus.gov/arrhythmia.html

Subscription / membership required

Full Text Sources:

MeSH Terms: Arrhythmias, Cardiac, Calsequestrin, Heterozygote, Humans, Mutation, Ryanodine Receptor Calcium Release Channel