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GENATLAS PHENOTYPE

last update : 28/12/06

Symbol	SQT3
Location	17q24.3
Name	short QT syndrome-3
Corresponding gene	KCNJ2
Main clinical features	markedly short repolarization time and conspicuously narrow and peaked T waves , with presyncopal episodes and palpitations, predisposing patients to life-threatening arrhythmias
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

Remark(s)