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Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

✍ Scribed by S.G Priori; C Napolitano; N Tiso


Book ID
114346623
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
49 KB
Volume
10
Category
Article
ISSN
1062-1458

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Involvement of the cardiac ryanodine rec
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## Abstract The cardiac ryanodine receptor (RyR2), the major calcium release channel on the sarcoplasmic reticulum (SR) in cardiomyocytes, has recently been shown to be involved in at least two forms of sudden cardiac death (SCD): (1) Catecholaminergic polymorphic ventricular tachycardia (CPVT) or