Cite
HARVARD Citation
Graziola, F. et al. (2019). A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder. Parkinsonism & related disorders. pp. 4-6. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Graziola, F. et al. (2019). A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder. Parkinsonism & related disorders. pp. 4-6. [Online].