Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish-Reference-Cited by-同舟云学术

Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish

Published:2016-03-10 Issue:3 Volume:11 Page:e0151148
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Grone Brian P.,Marchese Maria,Hamling Kyla R.,Kumar Maneesh G.,Krasniak Christopher S.,Sicca Federico,Santorelli Filippo M.,Patel Manisha,Baraban Scott C.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference80 articles.

1. De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy;H Saitsu;Nature genetics,2008

2. Folinic acid responsive epilepsy in Ohtahara syndrome caused by STXBP1 mutation;WW Tso;Pediatr Neurol,2014

3. STXBP1 mutations cause not only Ohtahara syndrome but also West syndrome—result of Japanese cohort study;M Otsuka;Epilepsia,2010

4. De novo mutations in epileptic encephalopathies;AS Allen;Nature,2013

5. GABRA1 and STXBP1: novel genetic causes of Dravet syndrome;GL Carvill;Neurology,2014

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