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...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Universitas Gadjah Mada
2017-03-01
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Series: | Journal of the Medical Sciences |
Subjects: | |
Online Access: | https://jurnal.ugm.ac.id/bik/article/view/19080 |