Epilepsy: GRIN2A mutations identified as key genetic drivers of epilepsy—aphasia spectrum disorders

Nature Reviews Neurology

Volumn 9, Issue 10, 2013, Pages 541-

  Kingwell, Katie ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

N METHYL DEXTRO ASPARTIC ACID RECEPTOR;

FEMALE; FOCAL EPILEPSY; GENETICS; HUMAN; LANDAU KLEFFNER SYNDROME; MALE; MUTATION; NOTE;

EPILEPSIES, PARTIAL; FEMALE; HUMANS; LANDAU-KLEFFNER SYNDROME; MALE; MUTATION; RECEPTORS, N-METHYL-D-ASPARTATE;

EID: 84899783677     PISSN: 17594758     EISSN: 17594766     Source Type: Journal    
DOI: 10.1038/nrneurol.2013.181     Document Type: Article

References (4)

1. Lemke, J. R. et al. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nat. Genet. doi:10.1038/ng.2728
2. Lesca, G. et al. GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nat. Genet. doi:10.1038/ng.2726
3. Carvill, G. L. et al. GRIN2A mutations cause epilepsy-aphasia spectrum disorders. Nat. Genet. doi:10.1038/ng.2727
4. Epik4 Consortium & Epilepsy Phenome/Genome Project. De novo mutations in epileptic encephalopathies. Nature doi:10.1038/nature12439