Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference15 articles.
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2. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia;SG Priori;Circulation,2001
3. 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;H Lahat;Am J Hum Genet,2001
4. Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testing;DJ Tester;Heart Rhythm,2006
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