The α-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases

We report the results of a screen of 230 European familial index cases of Parkinson's disease for the recently described Ala53Thr mutation in the α‐synuclein gene in an autosomal dominant Parkinson's disease kindred. No mutations were found from this broad white population, and we therefor...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Annals of neurology 1998-08, Vol.44 (2), p.270-273
Hauptverfasser:	Vaughan, Jenny, Durr, Alexandra, Tassin, Johann, Bereznai, Benjamin, Gasser, Thomas, Bonifati, Vincenzo, De Michele, Giuseppe, Fabrizio, Edito, Volpe, Gianpiero, Bandmann, O., Johnson, William G., Golbe, Lawrence I., Breteler, Monique, Meco, Giuseppe, Agid, Yves, Brice, Alexis, Marsden, C. David, Wood, Nicholas W.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Medical sciences Neurology
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!