@article {1950,
	title = {A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.},
	journal = {Pediatr Neurol},
	volume = {47},
	year = {2012},
	month = {2012 Aug},
	pages = {133-6},
	abstract = {<p>Hemiplegic migraine constitutes an unusual form, characterized by periodic attacks of migraine with a motor component (hemiplegia). Familial forms are dominantly inherited, and are attributable to mutations in genes encoding proteins involved in ion transportation, including ATP1A2, which codes for the α-2 isoform of the sodium-potassium adenosine triphosphatase, a P-type cation transport adenosine triphosphatase, and responsible for the so-called familial hemiplegic migraine type 2. We describe a 9-year-old boy affected by familial hemiplegic migraine, with a novel ATP1A2 gene mutation (c.1799T>C p.V600A) in exon 13. Long-term treatment with flunarizine resulted in a good clinical response and the prevention of further attacks.</p>},
	keywords = {Amino Acid Sequence, Child, Preschool, Humans, Male, Migraine with Aura, Molecular Sequence Data, Mutation, Pedigree, Sodium-Potassium-Exchanging ATPase},
	issn = {1873-5150},
	doi = {10.1016/j.pediatrneurol.2012.04.012},
	author = {De Cunto, Angela and Bensa, Marco and Tonelli, Alessandra}
}
