Phenotypic analysis of 303 multiplex families with common epilepsies
Author:
Funder
NIH
NHMRC
HRC
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/140/8/2144/25417299/awx129.pdf
Reference71 articles.
1. Multiplex families with epilepsy: success of clinical and molecular genetic characterization;Afawi;Neurology,2016
2. Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency;Arsov;Epilepsia,2012
3. A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33;Baulac;Am J Hum Genet,1999
4. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005–2009;Berg;Epilepsia,2010
5. Epilepsies in twins: genetics of the major epilepsy syndromes;Berkovic;Ann Neurol,1998
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