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, AlessandroVolume:
76
Journal:
Parkinsonism & Related Disorders
DOI:
10.1016/j.parkreldis.2020.06.001
Date:
July, 2020
File:
PDF, 573 KB
2020