No association of DNM3 with age of onset in Asian Parkinson's disease

Background and purpose Genetic variability in DNM3 has been shown to modify age of onset of Parkinson's disease (PD) among LRRK2 Gly2019Ser carriers in North African Arab–Berber populations. In Asian populations, the Gly2019Ser mutation is rare or absent but two other LRRK2 variants, Gly2385Arg...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	European journal of neurology 2019-05, Vol.26 (5), p.827-829
Hauptverfasser:	Foo, J. N., Tan, L. C., Au, W.‐L., Prakash, K.‐M., Liu, J., Tan, E.‐K.
Format:	Artikel
Sprache:	eng
Schlagworte:	Age age of onset Genetic variability Genotypes Heterogeneity human genetics LRRK2 protein modifiers Movement disorders Mutation Neurodegenerative diseases Parkinson's disease Populations Risk
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!