CHD2 mutations are a rare cause of generalized epilepsy with myoclonic–atonic seizures-Reference-Cited by-同舟云学术

CHD2 mutations are a rare cause of generalized epilepsy with myoclonic–atonic seizures

Published:2015-10 Issue: Volume:51 Page:53-56
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Trivisano Marina,Striano Pasquale,Sartorelli Jacopo,Giordano Lucio,Traverso Monica,Accorsi Patrizia,Cappelletti Simona,Claps Dianela Judith,Vigevano Federico,Zara Federico,Specchio Nicola

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Neurology (clinical),Neurology

Reference18 articles.

1. Delineation of cryptogenic Lennox–Gastaut syndrome and myoclonic astatic epilepsy using multiple correspondence analysis;Kaminska;Epilepsy Res,1999

2. Myoclonic astatic epilepsy: an age-dependent epileptic syndrome with favorable seizure outcome but variable cognitive evolution;Trivisano;Epilepsy Res,2011

3. Centrencephalic myoclonic–astatic petit mal;Doose;Neuropediatrics,1970

4. Dissecting the genetic basis of myoclonicastatic epilepsy;Tang;Epilepsia,2012

5. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1;Carvill;Nat Genet,2013

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