A missense mutation in the CASQ2 gene is associated with autosomal-recessive catecholamine-induced polymorphic ventricular tachycardia

Michael Eldar; Elon Pras; Hadas Lahat

doi:10.1016/S1050-1738(03)00025-2

A missense mutation in the CASQ2 gene is associated with autosomal-recessive catecholamine-induced polymorphic ventricular tachycardia

Michael Eldar^*, Elon Pras, Hadas Lahat

^*Corresponding author for this work

Research output: Contribution to journal › Review article › peer-review

Abstract

Catecholamine-induced polymorphic ventricular tachycardia (CPVT), a rare disease that occurs in subjects without obvious organic heart disease, is characterized by episodes of syncope, seizures, or sudden death in response to physiologic or emotional stress. This report reviews evidence that a missense mutation in the CASQ2 gene is associated with autosomal-recessive CPVT.

Original language	English
Pages (from-to)	148-151
Number of pages	4
Journal	Trends in Cardiovascular Medicine
Volume	13
Issue number	4
DOIs	https://doi.org/10.1016/S1050-1738(03)00025-2
State	Published - May 2003
Externally published	Yes

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10.1016/S1050-1738(03)00025-2

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title = "A missense mutation in the CASQ2 gene is associated with autosomal-recessive catecholamine-induced polymorphic ventricular tachycardia",

abstract = "Catecholamine-induced polymorphic ventricular tachycardia (CPVT), a rare disease that occurs in subjects without obvious organic heart disease, is characterized by episodes of syncope, seizures, or sudden death in response to physiologic or emotional stress. This report reviews evidence that a missense mutation in the CASQ2 gene is associated with autosomal-recessive CPVT.",

author = "Michael Eldar and Elon Pras and Hadas Lahat",

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AB - Catecholamine-induced polymorphic ventricular tachycardia (CPVT), a rare disease that occurs in subjects without obvious organic heart disease, is characterized by episodes of syncope, seizures, or sudden death in response to physiologic or emotional stress. This report reviews evidence that a missense mutation in the CASQ2 gene is associated with autosomal-recessive CPVT.

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JO - Trends in Cardiovascular Medicine

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A missense mutation in the CASQ2 gene is associated with autosomal-recessive catecholamine-induced polymorphic ventricular tachycardia

Abstract

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