Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case report
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DOI: 10.1186/s12888-018-1822-8
Abstract: BackgroundMutations in voltage-gated sodium channel (SCN) genes are supposed to be of importance in the etiology of psychiatric and neurological diseases, in particular in the etiology of seizures. Previous studies report a potential susceptibility region… read more here.
Keywords: scn2a scn3a; etiology; scn2a; case ... See more keywords