Citations for
1MHP2, ATP1A2, AHPC
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood.
Bassi MT, Bresolin N, Tonelli A, Nazos K, Crippa F, Baschirotto C, Zucca C, Bersano A, Dolcetta D, Boneschi FM, Barone V, Casari G.
J Med Genet 41(8):621-8. No abstract available. 2004
2AHPC, ATP1A2
Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.
Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE, Leppert MF, Schlesinger-Massart MB, Ptacek LJ, Silver K, Youroukos S.
Ann Neurol 55(6):884-7. 2004
3AHPC, ATP1A2
Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait.
Kanavakis E, Xaidara A, Papathanasiou-Klontza D, Papadimitriou A, Velentza S, Youroukos S.
Dev Med Child Neurol 45(12):833-6. Erratum in: Dev Med Child Neurol. 2004 Apr;46(4):288. 2003