Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy-Reference-Cited by-同舟云学术

Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy

Published:2012-06-12 Issue:8 Volume:53 Page:e146-e150
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Poduri Annapurna,Chopra Sameer S.,Neilan Edward G.,Christina Elhosary P.,Kurian Manju A.,Meyer Esther,Barry Brenda J.,Khwaja Omar S.,Salih Mustafa A. M.,Stödberg Tommy,Scheffer Ingrid E.,Maher Eamonn R.,Sahin Mustafa,Wu Bai-Lin,Berry Gerard T.,Walsh Christopher A.,Picker Jonathan,Kothare Sanjeev V.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2012.03538.x/fullpdf

Reference11 articles.

1. Duplication 16p11.2 in a child with infantile seizure disorder;Bedoyan;Am J Med Genet A,2010

2. De novo SCN1A mutations in migrating partial seizures of infancy;Carranza Rojo;Neurology,2011

3. Migrating partial seizures in infancy: a malignant disorder with developmental arrest;Coppola;Epilepsia,1995

4. Novel SCN1A mutation in a proband with malignant migrating partial seizures of infancy;Freilich;Arch Neurol,2011

5. Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes;Heinzen;Am J Hum Genet,2010

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