Rare gene deletions in genetic generalized and Rolandic epilepsies

Author:

Jabbari KamelORCID,Bobbili Dheeraj R.,Lal Dennis,Reinthaler Eva M.,Schubert Julian,Wolking StefanORCID,Sinha Vishal,Motameny Susanne,Thiele Holger,Kawalia AmitORCID,Altmüller Janine,Toliat Mohammad Reza,Kraaij Robert,van Rooij JeroenORCID,Uitterlinden André G.,Ikram M. ArfanORCID,Zara Federico,Lehesjoki Anna-Elina,Krause RolandORCID,Zimprich FritzORCID,Sander Thomas,Neubauer Bernd A.,May PatrickORCID,Lerche Holger,Nürnberg PeterORCID,

Funder

DFG

NOW

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference83 articles.

1. Estimating risk for developing epilepsy;DC Hesdorffer;Neurology,2011

2. Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy;KL Helbig;Genet Med Off J Am Coll Med Genet,2016

3. A genomic view on epilepsy and autism candidate genes;K Jabbari;Genomics,2016

4. De novo mutations in epileptic encephalopathies;AS Allen;Nature,2013

5. Epilepsy and Autism;AW Buckley;Cold Spring Harb Perspect Med,2016

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