Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy

J Neurol Sci. 2021 Nov 15:430:120031. doi: 10.1016/j.jns.2021.120031. Epub 2021 Oct 16.

¹ Institute for Biomedical Research and Innovation, National Research Council, Mangone, CS, Italy. Electronic address: monicg_2002@yahoo.it.
² Institute of Neurology, Department of Medical and Surgical Sciences, University Magna Graecia, Catanzaro, Italy.
³ Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto, Catanzaro, Italy.
⁴ Department of Neurology, Milan Center for Neuroscience, San Gerardo Hospital, University of Milano-Bicocca, Monza, Italy.
⁵ Department of Medical and Surgical Science, Pediatrics Unit, University Magna Graecia, Catanzaro, Italy.
⁶ Laboratory of Molecular Oncology, Department of Experimental and Clinical Medicine, Magna Graecia University, Catanzaro, Italy; Interdepartmental Center of Services (CIS), Magna Graecia University, Catanzaro, Italy.
⁷ Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto, Catanzaro, Italy; Neuroscience Center, University Magna Graecia, Catanzaro, Italy.
⁸ Institute for Biomedical Research and Innovation, National Research Council, Mangone, CS, Italy.

No abstract available

Keywords: ATP13A2; Autosomal recessive form; Multiple system atrophy; Parkinson's disease.

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