Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region-Reference-Cited by-同舟云学术

Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region

Published:2010-04-02 Issue:9 Volume:51 Page:1870-1873
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Reutlinger Constanze,Helbig Ingo,Gawelczyk Barbara,Subero Jose Ignacio Martin,Tönnies Holger,Muhle Hiltrud,Finsterwalder Katrin,Vermeer Sascha,Pfundt Rolph,Sperner Jürgen,Stefanova Irina,Gillessen-Kaesbach Gabriele,Von Spiczak Sarah,Van Baalen Andreas,Boor Rainer,Siebert Reiner,Stephani Ulrich,Caliebe Almuth

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2010.02555.x/fullpdf

Reference9 articles.

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3. 4-Aminobutyrate aminotransferase (GABA-transaminase) deficiency;Medina-Kauwe;J Inherit Metab Dis,1999

4. Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14;Neubauer;Neurology,1998

5. KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes;Neubauer;Neurology,2008

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