Parkinsonism in GTP cyclohydrolase 1 mutation carriers
- PMID: 25497597
- PMCID: PMC5963401
- DOI: 10.1093/brain/awu341
Parkinsonism in GTP cyclohydrolase 1 mutation carriers
Comment in
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Reply: Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.Brain. 2015 May;138(Pt 5):e352. doi: 10.1093/brain/awu309. Epub 2014 Nov 14. Brain. 2015. PMID: 25398234 Free PMC article. No abstract available.
Comment on
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Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.Brain. 2014 Sep;137(Pt 9):2480-92. doi: 10.1093/brain/awu179. Epub 2014 Jul 2. Brain. 2014. PMID: 24993959 Free PMC article.
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- Furukawa Y, Lang AE, Trugman JM, Bird TD, Hunter A, Sadeh M, et al. Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystonia. Neurology. 1998;50:1015–20. - PubMed
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- Hertz JM, Ostergaard K, Juncker I, Pedersen S, Romstad A, Moller LB, et al. Low frequency of Parkin, tyrosine hydroxylase, and GTP cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease. Eur J Neurol. 2006;13:385–90. - PubMed
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- Hjermind LE, Johannsen LG, Blau N, Wevers RA, Lucking CB, Hertz JM, et al. Dopa-responsive dystonia and early-onset Parkinson's disease in a patient with GTP cyclohydrolase I deficiency? Mov Disord. 2006;21:679–82. - PubMed
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