Parkinsonism in GTP cyclohydrolase 1-deficient DOPA-responsive dystonia.
Identifieur interne : 000595 ( Main/Exploration ); précédent : 000594; suivant : 000596Parkinsonism in GTP cyclohydrolase 1-deficient DOPA-responsive dystonia.
Auteurs : Yoshiaki Furukawa [Japon] ; Stephen J. Kish [Canada]Source :
- 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/awu325
PubMed: 25416181
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream Ncbi, to step Merge: 001969
- to stream Ncbi, to step Curation: 001969
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Le document en format XML
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<country wicri:rule="url">Japon</country>
<wicri:regionArea>1 Department of Neurology, Juntendo Tokyo Koto Geriatric Medical Center, Tokyo, Japan 2 Department of Neurology, Faculty of Medicine, University and Postgraduate University of Juntendo, Tokyo</wicri:regionArea>
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<term>Parkinson Disease (diagnosis)</term>
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