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Both gain-of-function and loss-of-function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox-Gastaut syndrome

Xiao Jiang, Praveen K. Raju, Nazzareno D'Avanzo, Mathieu Lachance, Julie Pepin, François Dubeau, Wendy G. Mitchell, Luis E. Bello-Espinosa, Tyler M. Pierson, Berge A. Minassian, Jean Claude Lacaille, Elsa Rossignol

Research output: Contribution to journal › Article › peer-review

58 Scopus citations

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Medicine & Life Sciences