A New Mutation in the Ryanodine Receptor 2 Gene (RYR2 C2277R) as a Cause Catecholaminergic Polymorphic Ventricular Tachycardia

Saved in:
Bibliographic Details
Published in:Revista española de cardiología (English ed.) 2015-01, Vol.68 (1), p.71-73
Main Authors: Domingo, Diana, López-Vilella, Raquel, Arnau, Miguel Ángel, Cano, Óscar, Fernández-Pons, Elena, Zorio, Esther
Format: Article
Language:English
Subjects:
Adolescent
Adult
Child
DNA - genetics
DNA Mutational Analysis
Female
Humans
Male
Middle Aged
Mutation
Pedigree
Ryanodine Receptor Calcium Release Channel - genetics
Ryanodine Receptor Calcium Release Channel - metabolism
Tachycardia, Ventricular - genetics
Tachycardia, Ventricular - metabolism
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:1885-5857
1885-5857
DOI:10.1016/j.rec.2014.07.022