Common polymorphism in scn5a implicated in drug-induced...

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

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C435S007100, C435S252300, C435S254200, C435S320100, C435S325000, C435S348000, C435S349000, C435S358000, C435S363000, C435S365000, C435S367000, C435S419000, C435S455000, C530S350000, C536S023500

Reexamination Certificate

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10333191

ABSTRACT:
The present invention is directed to a specific mutation in SCN5A which causes drug-induced torsade de pointes or ventricular fibrillation. Persons with the mutation are predisposed to developing drug-induced torsade de pointes or ventricular fibrillation when administered certain drugs. This predisposition can be diagnosed in accordance with the present invention by analyzing the DNA sequence of the SCN5A of an individual. By screening patients for the mutation, drug-induced torsade de pointes or ventricular fibrillation can be avoided. Furthermore, drugs can be tested to determine whether they will cause torsade de pointes or ventricular fibrillation.

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