GRIN2A mutations cause epilepsy-aphasia spectrum disorders-Reference-Cited by-同舟云学术

GRIN2A mutations cause epilepsy-aphasia spectrum disorders

Published:2013-08-11 Issue:9 Volume:45 Page:1073-1076
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Carvill Gemma L,Regan Brigid M,Yendle Simone C,O'Roak Brian J,Lozovaya Natalia,Bruneau Nadine,Burnashev Nail,Khan Adiba,Cook Joseph,Geraghty Eileen,Sadleir Lynette G,Turner Samantha J,Tsai Meng-Han,Webster Richard,Ouvrier Robert,Damiano John A,Berkovic Samuel F,Shendure Jay,Hildebrand Michael S,Szepetowski Pierre,Scheffer Ingrid E,Mefford Heather C

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2727.pdf

Reference19 articles.

1. Berg, A.T. et al. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005–2009. Epilepsia 51, 676–685 (2010).

2. Tassinari, C.A. et al. Encephalopathy with electrical status epilepticus during slow sleep or ESES syndrome including the acquired aphasia. Clin. Neurophysiol. 111 (suppl. 2), S94–S102 (2000).

3. Tsai, M.H. et al. Clinical genetic study of the epilepsy-aphasia spectrum. Epilepsia 54, 280–287 (2013).

4. Deonna, T.W., Roulet, E., Fontan, D. & Marcoz, J.P. Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome. Neuropediatrics 24, 83–87 (1993).

5. Scheffer, I.E. et al. Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipation. Ann. Neurol. 38, 633–642 (1995).

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