Myoclonic epilepsy of infancy related to YWHAG gene mutation: towards a better phenotypic characterization

Seizure. 2022 Jan:94:161-164. doi: 10.1016/j.seizure.2021.12.002. Epub 2021 Dec 8.

¹ Child Neuropsychiatry Unit, S. Chiara Hospital, APSS, Trento, Italy. Electronic address: alessandro.iodice@apss.tn.it.
² Child Neuropsychiatry Unit, S. Chiara Hospital, APSS, Trento, Italy.
³ Medical Genetic Unit, S. Chiara Hospital APSS, Trento, Italy.
⁴ Paediatric Neurology and Muscular Disease Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.

No abstract available

Keywords: Gene developmental and epileptic enchephalopathy; Myoclonic Epilepsy; Neurodevelopmental disorders; YWHAG.

MeSH terms