Cite
HARVARD Citation
Ban, R. et al. (2021). A novel homozygous mutation in ATP13A2 gene causing pure hereditary spastic paraplegia. Parkinsonism & related disorders. pp. 58-60. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Ban, R. et al. (2021). A novel homozygous mutation in ATP13A2 gene causing pure hereditary spastic paraplegia. Parkinsonism & related disorders. pp. 58-60. [Online].