| Literature DB >> 23182416 |
Young Ok Kim1, Leanne Dibbens, Carla Marini, Arvid Suls, Nicole Chemaly, Davide Mei, Jacinta M McMahon, Xenia Iona, Samuel F Berkovic, Peter De Jonghe, Renzo Guerrini, Rima Nabbout, Ingrid E Scheffer.
Abstract
A homozygous SCN1B mutation was previously identified in a patient with early onset epileptic encephalopathy (EOEE) described as Dravet syndrome (DS) despite a more severe phenotype than DS. We investigated whether SCN1B mutations are a common cause of DS. Patients with DS who did not have a SCN1A sequencing mutation or copy number variation were studied. Genomic DNA was Sanger sequenced for mutations in the 6 exons of SCN1B. In 54 patients with DS recruited from four centres, no SCN1B mutations were identified. SCN1B mutation is not a common cause of DS.Entities:
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Year: 2012 PMID: 23182416 DOI: 10.1016/j.eplepsyres.2012.10.009
Source DB: PubMed Journal: Epilepsy Res ISSN: 0920-1211 Impact factor: 3.045