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De novo SCN1A, SCN8A, and CLCN2 mutations in childhood absence epilepsy

  • Published:2019-08 Issue: Volume:154 Page:55-61
  • ISSN:0920-1211
  • Container-title:Epilepsy Research
  • language:en
  • Short-container-title:Epilepsy Research

Author:

Xie Han,Su Wenting,Pei Jinrui,Zhang Yujia,Gao Kai,Li Jinliang,Ma Xiuwei,Zhang Yuehua,Wu Xiru,Jiang Yuwu

Funder

National Natural Science Foundation of China

Beijing Natural Science Foundation

Beijing Municipal Science & Technology Commission

Beijing Institute for Brain Disorders Foundation

Beijing Municipal Natural Science Key Project

Beijing key laboratory of molecular diagnosis and study on pediatric genetic diseases

National Key Research and Development Program of China

Fundamental Research Funds for the Central Universities

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference37 articles.

1. Clinical dissection of early onset absence epilepsy in children and prognostic implications;Agostinelli;Epilepsia,2013

2. Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution;Agostinelli;Eur. J. Neurol.,2013

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

4. Toward the estimation of the absolute quality of individual protein structure models;Benkert;Bioinformatics,2011

5. Modeling protein quaternary structure of homo- and hetero-oligomers beyond binary interactions by homology;Bertoni;Sci. Rep.,2017

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