GTP cyclohydrolase 1 mutations and Parkinson's disease: new insights beyond DOPA-responsive dystonia.
Identifieur interne : 000230 ( Main/Exploration ); précédent : 000229; suivant : 000231GTP cyclohydrolase 1 mutations and Parkinson's disease: new insights beyond DOPA-responsive dystonia.
Auteurs : Miryam Carecchio [Italie] ; Susanne A. Schneider [Allemagne]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : GTP Cyclohydrolase.
- diagnosis : Parkinson Disease.
- genetics : Mutation, Parkinson Disease.
- Female, Heterozygote, Humans, Male.
DOI: 10.1002/mds.26283
PubMed: 26012785
Affiliations:
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Le document en format XML
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<affiliation wicri:level="3"><nlm:affiliation>Molecular Neurogentics Unit, C. Besta Institute, Milan, Italy.</nlm:affiliation>
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<author><name sortKey="Schneider, Susanne A" sort="Schneider, Susanne A" uniqKey="Schneider S" first="Susanne A" last="Schneider">Susanne A. Schneider</name>
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