Article
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy.
Epilepsia - 1 Aug 2014
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
Abstract excerpt
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 postulated to confer susceptibility to parts of the disease spectrum: the ELP4 gene to centrotemporal spikes and SRPX2 to ARE. To...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.