CareLit · DOI-Nachweis · Aktuelle Neurologie
Sporadic hemiplegic migraine associated with a novel mutation in ATP1A2
DOI 10.1055/s-2006-953111
Bibliografische Angaben
Nachweis in CareLit
Autor:innenT. Freilinger, M. Popovici, N. Tavraz, T. Friedrich, M. Dichgans
ZeitschriftAktuelle Neurologie
Ausgabe09/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Aims: Familial hemiplegic migraine (FHM) is a rare autosomal-dominant subtype of migraine with aura (MA) characterized by some degree of hemiparesis during the aura; so far, mutations in three genes (CACNA1A, ATP1A2 and SCN1A) have been identified in FHM pedigrees. In sporadic hemiplegic migraine (SHM) (i.e. hemiplegic migraine without a history of affected family members) the role of these genes is less clear. Prev…
Zitieren
Zitierempfehlung
T. Freilinger, M. Popovici, N. Tavraz, T. Friedrich, M. Dichgans (2006) Sporadic hemiplegic migraine associated with a novel mutation in ATP1A2. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2006-953111
Mit CareLit weiterarbeiten