Reference : Familial basilar migraine associated with a new mutation in the ATP1A2 gene
Scientific journals : Article
Human health sciences : Neurology
http://hdl.handle.net/2268/23891
Familial basilar migraine associated with a new mutation in the ATP1A2 gene
English
Ambrosini, A. [> > > >]
D'Onofrio, M. [> > > >]
Grieco, G. S. [> > > >]
Di Mambro, A. [> > > >]
Montagna, G. [> > > >]
Fortini, D. [> > > >]
Nicoletti, F. [> > > >]
Nappi, G. [> > > >]
Sances, G. [> > > >]
Schoenen, Jean mailto [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Neuro-anatomie]
Buzzi, M. G. [> > > >]
Santorelli, F. M. [> > > >]
Pierelli, F. [> > > >]
13-Dec-2005
Neurology
Lippincott Williams & Wilkins
65
11
1826-1828
Yes (verified by ORBi)
International
0028-3878
Philadelphia
[en] Basilar migraine (BM), familial hemiplegic migraine (FHM), and sporadic hemiplegic migraine (SHM) are phenotypically similar subtypes of migraine with aura, differentiated only by motor symptoms, which are absent in BM. Mutations in CACNA1A and ATP1A2 have been found in FHM. The authors detected a novel mutation in the ATP1A2 gene (R548H) in members of a family with BM, suggesting that BM and FHM may be allelic disorders.
http://hdl.handle.net/2268/23891

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