SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations

Published 2016 View Full Article

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Title
SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations
Authors
Keywords
Dravet syndrome, Epileptic encephalopathy, GEFS+, SCN1A mutation
Journal
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
Volume 39, Issue -, Pages 34-43
Publisher
Elsevier BV
Online
2016-05-21
DOI
10.1016/j.seizure.2016.05.008

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