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Pubmed ID :9024139
Publication Date : //

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome.


Familial long-QT syndrome (LQTS) is characterized by prolonged ventricular repolarization. Clinical symptoms include recurrent syncopal attacks, and sudden death may occur due to ventricular tachyarrhythmias. Three genes responsible for this syndrome (KVLQT1, HERG, and SCN5A) have been identified so far. We investigated mutations of these genes in LQTS families.

Authors : Tanaka T , Nagai R , Tomoike H , Takata S , Yano K , Yabuta K , Haneda N , Nakano O , Shibata A , Sawayama T , Kasai H , Yazaki Y , Nakamura Y ,

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