Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2...

Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation

De Michele, Giovanna, Galatolo, Daniele, Lieto, Maria, Fico, Tommasina, Saccà, Francesco, Santorelli, Filippo M., Filla, Alessandro
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Volume:
76
Journal:
Parkinsonism & Related Disorders
DOI:
10.1016/j.parkreldis.2020.06.001
Date:
July, 2020
File:
PDF, 573 KB
2020
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