Parkinsonism in GTP cyclohydrolase 1 mutation carriers.
Identifieur interne : 000504 ( PubMed/Corpus ); précédent : 000503; suivant : 000505Parkinsonism in GTP cyclohydrolase 1 mutation carriers.
Auteurs : Ilaria Guella ; Holly E. Sherman ; Silke Appel-Cresswell ; Alex Rajput ; Ali H. Rajput ; Matthew J. FarrerSource :
- Brain : a journal of neurology [ 1460-2156 ] ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : GTP Cyclohydrolase.
- diagnosis : Parkinson Disease.
- genetics : Mutation, Parkinson Disease.
- Female, Heterozygote, Humans, Male.
DOI: 10.1093/brain/awu341
PubMed: 25497597
Links to Exploration step
pubmed:25497597Le document en format XML
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<author><name sortKey="Guella, Ilaria" sort="Guella, Ilaria" uniqKey="Guella I" first="Ilaria" last="Guella">Ilaria Guella</name>
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<author><name sortKey="Sherman, Holly E" sort="Sherman, Holly E" uniqKey="Sherman H" first="Holly E" last="Sherman">Holly E. Sherman</name>
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<author><name sortKey="Appel Cresswell, Silke" sort="Appel Cresswell, Silke" uniqKey="Appel Cresswell S" first="Silke" last="Appel-Cresswell">Silke Appel-Cresswell</name>
<affiliation><nlm:affiliation>2 Pacific Parkinson's Research Centre, Department of Medicine (Neurology), University of British Columbia Vancouver, BC, Canada.</nlm:affiliation>
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<author><name sortKey="Rajput, Ali H" sort="Rajput, Ali H" uniqKey="Rajput A" first="Ali H" last="Rajput">Ali H. Rajput</name>
<affiliation><nlm:affiliation>3 Division of Neurology, University of Saskatchewan and Saskatoon Health Region, Saskatoon, SK, Canada.</nlm:affiliation>
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<term>Male</term>
<term>Mutation (genetics)</term>
<term>Parkinson Disease (diagnosis)</term>
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<ArticleTitle>Parkinsonism in GTP cyclohydrolase 1 mutation carriers.</ArticleTitle>
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