BRIEF REPORT: A novel ATP1A2 mutation in a family with FHM type II

Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura with an autosomal dominant pattern of inheritance. Six FHM families underwent extensive clinical and genetic investigation. The authors identified a novel ATP1A2 mutation (E700K) in three patients from one family. In the pati...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Cephalalgia 2006-03, Vol.26 (3), p.324-328
Hauptverfasser:	Pierelli, F, Grieco, G S, Pauri, F, Pirro, C, Fiermonte, G, Ambrosini, A, Costa, A, Buzzi, M G, Valoppi, M, Caltagirone, C, Nappi, G, Santorelli, F M
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!