Familial hemiplegic migraine: A ion channel disorder

At present, little information is available on the genetics of common migraines, most likely to be considered a multifactorial disease. Recently, the CACNA1A gene encoding the brain-specific P/Q type calcium channel alpha(1) subunit, has been cloned and mutations in this gene, located on chromosome...

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Veröffentlicht in:	Brain research bulletin 2001-10, Vol.56 (3-4), p.239-241
Hauptverfasser:	CARRERA, Paola, STENIRRI, Stefania, FERRARI, Maurizio, BATTISTINI, Stefania
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Calcium Channels - genetics Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Humans Medical sciences Migraine with Aura - genetics Mutation Neurology Trinucleotide Repeats
Online-Zugang:	Volltext
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