Parkinson's disease in GTP cyclohydrolase 1 mutation carriers

Journal article

Peer reviewed

Brent J Ryan, Mark J Crabtree, Keith M Channon and Richard Wade-Martins

Brain (London, England : 1878), Vol.138(Pt 5), pp.e348-U10

01/05/2015

PMCID: PMC5963397

PMID: 25398233

Abstract

Female

GTP Cyclohydrolase - genetics

Heterozygote

Humans

Male

Mutation - genetics

Parkinson Disease - diagnosis

Parkinson Disease - genetics

url

https://doi.org/10.1093/brain/awu308View

Published (Version of record)

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Title: Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
Creators: Brent J Ryan - University of Oxford
Mark J Crabtree - University of Oxford
Keith M Channon - University of Oxford
Richard Wade-Martins - University of Oxford
Publication Details: Brain (London, England : 1878), Vol.138(Pt 5), pp.e348-U10
Date published: 01/05/2015
Grant note: G0400144 / Medical Research Council G-0801 / Parkinson's UK RG/12/5/29576 / British Heart Foundation J-0901 / Parkinson's UK G0200482 / Medical Research Council
Identifiers: 99790461402346
Academic Unit: School of Biosciences
Language: English
Resource Type: Journal article