Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy

Summary Rolandic epilepsy (RE) and its atypical variants (atypical rolandic epilepsy, ARE) along the spectrum of epilepsy–aphasia disorders are characterized by a strong but largely unknown genetic basis. Two genes with a putative (ELP4) or a proven (SRPX2) function in neuronal migration were postul...

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Veröffentlicht in:	Epilepsia (Copenhagen) 2014-08, Vol.55 (8), p.e89-e93
Hauptverfasser:	Reinthaler, Eva M., Lal, Dennis, Jurkowski, Wiktor, Feucht, Martha, Steinböck, Hannelore, Gruber‐Sedlmayr, Ursula, Ronen, Gabriel M., Geldner, Julia, Haberlandt, Edda, Neophytou, Birgit, Hahn, Andreas, Altmüller, Janine, Thiele, Holger, Toliat, Mohammad R., Lerche, Holger, Nürnberg, Peter, Sander, Thomas, Neubauer, Bernd A., Zimprich, Fritz
Format:	Artikel
Sprache:	eng
Schlagworte:	Association Austria - epidemiology Canada - epidemiology Child CNV Epilepsy Epilepsy, Rolandic - diagnosis Epilepsy, Rolandic - epidemiology Epilepsy, Rolandic - genetics Female Gene Genes Genetic Variation - genetics Germany - epidemiology Humans Idiopathic focal childhood epilepsy Male Membrane Proteins Mutation Neoplasm Proteins Nerve Tissue Proteins - genetics Polymorphism, Single Nucleotide - genetics SNP
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