A novel ATP13A2 variant causing complicated hereditary spastic paraplegia

F Zhang, P Liu, J Li, Z Cen, W Luo - Neurological Sciences, 2024 - Springer
Background ATP13A2 is a monogenic causative gene of Parkinson's disease, whose
biallelic mutations can result in Kufor-Rakeb syndrome. Biallelic mutations in ATP13A2 have …
相关文章

A novel ATP13A2 variant causing complicated hereditary spastic paraplegia

F Zhang, P Liu, J Li, Z Cen… - … sciences: official journal …, 2024 - pubmed.ncbi.nlm.nih.gov
Background ATP13A2 is a monogenic causative gene of Parkinson's disease, whose
biallelic mutations can result in Kufor-Rakeb syndrome. Biallelic mutations in ATP13A2 have …

A novel ATP13A2 variant causing complicated hereditary spastic paraplegia.

F Zhang, P Liu, J Li, Z Cen, W Luo - … and of the Italian Society of …, 2024 - europepmc.org
Background ATP13A2 is a monogenic causative gene of Parkinson's disease, whose
biallelic mutations can result in Kufor-Rakeb syndrome. Biallelic mutations in ATP13A2 have …