G209A Mutation in the α-synuclein gene is rare and not associated with sporadic Parkinson's disease

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Movement disorders 1998-11, Vol.13 (6), p.970-971
Hauptverfasser:	Ho, Shu-Leong, Kung, Michelle H. W.
Format:	Artikel
Sprache:	eng
Schlagworte:	Age of Onset Biological and medical sciences Chromosome Mapping Chromosomes, Human, Pair 4 Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases DNA Mutational Analysis England Female Hong Kong Humans Male Medical sciences Neurology Parkinson Disease - genetics Point Mutation Polymerase Chain Reaction Tropical medicine
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!