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Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.

AuthorsBrent J Ryan, Mark J Crabtree, Keith M Channon, Richard Wade-Martins
JournalBrain : a journal of neurology (Brain) Vol. 138 Issue Pt 5 Pg. e348 (May 2015) ISSN: 1460-2156 [Electronic] England
PMID25398233 (Publication Type: Letter, Comment)
Chemical References
  • GTP Cyclohydrolase
Topics
  • Female
  • GTP Cyclohydrolase (genetics)
  • Heterozygote
  • Humans
  • Male
  • Mutation (genetics)
  • Parkinson Disease (diagnosis, genetics)

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