| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6011447 | Epilepsy & Behavior | 2015 | 4 Pages |
Abstract
Remarkable clinical heterogeneity can be found among family members carrying the same SCN1A gene mutation. Variable involvement of visual-motor abilities might represent a neuropsychological feature which needs to be further explored in other familial cases.
Keywords
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Neuroscience
Behavioral Neuroscience
Authors
Claudia Passamonti, Cristina Petrelli, Davide Mei, Nicoletta Foschi, Renzo Guerrini, Leandro Provinciali, Nelia Zamponi,