SCN1A exon 26 variants in epilepsy and migraine patients

SCN1A exon 26 variants in epilepsy and migraine patients

Epilepsy and migraine are common neurological diseases in many populations. Mutation of the voltage gated natrium channel Nav1.1 (SCN1A) are important causes of different genetic epilepsies and can also cause familial hemiplegic migraine (FHM-III). This study aimed to identify SCN1A gene variation i...

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Bibliographic Details
Main Authors: Nova Dian Lestari, Endang Mutiawati, Ahmad Hamim Sadewa, Hasan Sjahrir, . Syahrul, Dessy Rakhmawati Emril, . Harapan
Format: Article
Language:English
Published: Universitas Gadjah Mada 2017-03-01
Series:Journal of the Medical Sciences
Subjects:
epilepsy - gene variation - migraine - mutation - scn1a
Online Access:https://jurnal.ugm.ac.id/bik/article/view/19080

Internet

https://jurnal.ugm.ac.id/bik/article/view/19080

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