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Case Reports
. 2020 Jul:76:42-43.
doi: 10.1016/j.parkreldis.2020.06.001. Epub 2020 Jun 7.

Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation

Giovanna De Michele  1 , Daniele Galatolo  2 , Maria Lieto  1 , Tommasina Fico  1 , Francesco Saccà  1 , Filippo M Santorelli  2 , Alessandro Filla  3
Affiliations
Case Reports

Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation

Giovanna De Michele et al. Parkinsonism Relat Disord. 2020 Jul.
No abstract available

Keywords: ATP13A2; Ataxia; Kufor-Rakeb syndrome; Myoclonus.

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