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Case Reports
. 2019 Aug:65:272-273.
doi: 10.1016/j.parkreldis.2019.05.025. Epub 2019 May 23.

From PARK9 to SPG78: The clinical spectrum of ATP13A2 mutations

Roberto Erro  1 , Marina Picillo  2 , Renzo Manara  2 , Maria Teresa Pellecchia  2 , Paolo Barone  2
Affiliations
Case Reports

From PARK9 to SPG78: The clinical spectrum of ATP13A2 mutations

Roberto Erro et al. Parkinsonism Relat Disord. 2019 Aug.
No abstract available

Keywords: Dystonia; Hereditary spastic paraplegia; Kufor Rakeb syndrome; Neuronal ceroid lipofuscinosis; Parkinsonism.

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