Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation
- PMID: 32559632
- DOI: 10.1016/j.parkreldis.2020.06.001
Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation
Keywords: ATP13A2; Ataxia; Kufor-Rakeb syndrome; Myoclonus.
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