Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy

Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy

Juvenile myoclonic epilepsy (JME) accounts for 26% of generalized idiopathic epileptic syndromes. The highest levels of thrombin activity are closely involved in the development of neurological diseases, including epilepsy. The prothrombin c.20210G>A (rs1799963) variation, which alters prothrombi...

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Bibliographic Details
Main Authors: João Paulo Lopes Born, Bruna Priscila dos Santos, Rodrigo Secolin, Fernando Tenório Gameleira, Tiago Gomes de Andrade, Luciana Cláudia Herculano Machado, Lívia Leite Góes Gitaí, Daniel Leite Góes Gitaí
Format: Article
Language:English
Published: Academia Brasileira de Neurologia (ABNEURO) 2015-04-01
Series:Arquivos de Neuro-Psiquiatria
Subjects:
polimorfismo
protrombina
epilepsia mioclônica juvenil
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2015000400289&lng=en&tlng=en

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