Reply: Parkinson's disease in GTP cyclohydrolase 1 mutation carriers. [electronic resource]
- Brain : a journal of neurology May 2015
- e352 p. digital
Publication Type: Letter; Comment
1460-2156
10.1093/brain/awu309 doi
Female GTP Cyclohydrolase--genetics Heterozygote Humans Male Mutation--genetics Parkinson Disease--diagnosis