Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6010490 | Epilepsy & Behavior | 2015 | 4 Pages |
Abstract
Chromodomain-helicase-DNA-binding protein 2 is not the major gene associated with MAE. Conversely, CHD2 could be responsible for a proper phenotype characterized by infantile-onset generalized epilepsy, intellectual disability, and photosensitivity, which might overlap with MAE, Lennox-Gastaut, Dravet, and Jeavons syndromes.
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Authors
Marina Trivisano, Pasquale Striano, Jacopo Sartorelli, Lucio Giordano, Monica Traverso, Patrizia Accorsi, Simona Cappelletti, Dianela Judith Claps, Federico Vigevano, Federico Zara, Nicola Specchio,