NaV1.2 haploinsufficiency in Scn2a knock-out mice causes an autistic-like phenotype attenuated with age
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DOI: 10.1038/s41598-019-49392-7
Abstract: Mutations of the SCN2A gene, encoding the voltage gated sodium channel NaV1.2, have been associated to a wide spectrum of epileptic disorders ranging from benign familial neonatal-infantile seizures to early onset epileptic encephalopathies such as… read more here.
Keywords: scn2a mice; knock mice; autistic like; scn2a ... See more keywords