Sporadic hemiplegic migraine with novel missense mutation in the SCN1A gene and positive response to anti-CGRP antibody: a case report.

Maria D'ApolitoMarianna Gabriella RispoliPaola AjdinajDaniela TravagliniLaura Bonanni

Published in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2024)

Keyphrases

late onset
intellectual disability
copy number
genome wide
cerebral palsy
genome wide identification
autism spectrum disorder
early onset
transcription factor
genome wide analysis