| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6022758 | Neurobiology of Disease | 2011 | 9 Pages |
Abstract
âºMutations of KCNJ10 contribute to autism with seizures and intellectual disability âºFunctionally, these mutations act through a gain-of-function of the Kir4.1 channel âºThe phenotype suggests that mutations affect K+ homeostasis mainly in the brain
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Authors
Federico Sicca, Paola Imbrici, Maria Cristina D'Adamo, Francesca Moro, Fabrizia Bonatti, Paola Brovedani, Alessandro Grottesi, Renzo Guerrini, Gabriele Masi, Filippo Maria Santorelli, Mauro Pessia,