The Phenotype of a CASQ2 Mutation in a Saudi Family with Catecholaminergic Polymorphic Ventricular Tachycardia
Author:
Affiliation:
1. Department of Genetics
2. Heart Center; King Faisal Specialist Hospital & Research Centre; Riyadh; Saudi Arabia
Publisher
Wiley
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1540-8159.2012.03434.x/fullpdf
Reference5 articles.
1. Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients;Leenhardt;Circulation,1995
2. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia;Laitinen;Circulation,2001
3. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia;Priori;Circulation,2001
4. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel;Lahat;Am J Hum Genet,2001
5. A simple salting out procedure for extracting DNA from human nucleated cells;Miller;Nucleic Acids Res,1988
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3. An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2 -Catecholaminergic Polymorphic Ventricular Tachycardia;Circulation;2020-09-08
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