Parkinsonism in GTP cyclohydrolase 1-deficient DOPA-responsive dystonia.
Identifieur interne : 000505 ( PubMed/Curation ); précédent : 000504; suivant : 000506Parkinsonism 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
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pubmed:25416181Le document en format XML
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<author><name sortKey="Furukawa, Yoshiaki" sort="Furukawa, Yoshiaki" uniqKey="Furukawa Y" first="Yoshiaki" last="Furukawa">Yoshiaki Furukawa</name>
<affiliation wicri:level="1"><nlm:affiliation>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, Japan furukawa@juntendo.gmc.ac.jp.</nlm:affiliation>
<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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<author><name sortKey="Kish, Stephen J" sort="Kish, Stephen J" uniqKey="Kish S" first="Stephen J" last="Kish">Stephen J. Kish</name>
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