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FODSTAD , Heidi

Last name: FODSTAD

First name: Heidi

2006 (v1)

Journal article

Metadata-only

Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.

Fodstad, Heidi Bendahhou, Saïd Rougier, Jean-Sébastien

BACKGROUND: Mutations of at least six different genes have been found to cause long QT syndrome (LQTS), an inherited arrhythmic disorder characterized by a prolonged QT interval on the electrocardiogram (ECG), ventricular arrhythmias and risk of sudden death. AIM: The aims were to define the yet undetermined phenotypic characteristics of two...

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