Cite
HARVARD Citation
Zimmermann, M. et al. (2018). Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism. Parkinsonism & related disorders. pp. 145-147. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Zimmermann, M. et al. (2018). Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism. Parkinsonism & related disorders. pp. 145-147. [Online].