Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies-Reference-Cited by-同舟云学术

Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies

Published:2018-01-26 Issue:8 Volume:17 Page:e12456
ISSN:1601-1848
Container-title:Genes, Brain and Behavior
language:en
Short-container-title:Genes, Brain and Behavior

Author:

Zhou P.¹²,He N.¹²,Zhang J.-W.³,Lin Z.-J.¹²,Wang J.¹²,Yan L.-M.¹²,Meng H.⁴⁵,Tang B.¹²,Li B.-M.¹²,Liu X.-R.¹²,Shi Y.-W.¹²,Zhai Q.-X.³,Yi Y.-H.¹²,Liao W.-P.¹²^ORCID

Affiliation:

1. Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University; Institute of Neuroscience; Guangzhou China

2. Key Laboratory of Neurogenetics; Channelopathies of Guangdong Province and the Ministry of Education of China; Guangzhou China

3. Department of Pediatrics, Guangdong General Hospital; Guangdong Academy of Medical Sciences; Guangzhou China

4. Department of Neurology; The First Affiliated Hospital of Jinan University; Guangzhou China

5. Clinical Neuroscience Institute; Jinan University; Guangzhou China

Funder

Natural Science Foundation of Guangdong Province

Science and Technology Project of Guangzhou

Ministry of Science and Technology of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Behavioral Neuroscience,Neurology,Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/gbb.12456/fullpdf

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2. A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE task force on classification and terminology;Jerome Engel;Epilepsia,2001

3. The genetic landscape of the epileptic encephalopathies of infancy and childhood;McTague;Lancet Neurol,2016

4. Epilepsy-associated genes;Wang;Seizure,2017

5. Severe myoclonic epilepsy in infancy: Dravet syndrome;Dravet;Adv Neurol,2005

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