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

作者信息

De Michele Giovanna, Galatolo Daniele, Lieto Maria, Fico Tommasina, Saccà Francesco, Santorelli Filippo M, Filla Alessandro

机构信息

Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.

Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Fondazione Stella Maris, Pisa, Italy.

出版信息

Parkinsonism Relat Disord. 2020 Jul;76:42-43. doi: 10.1016/j.parkreldis.2020.06.001. Epub 2020 Jun 7.

DOI:10.1016/j.parkreldis.2020.06.001
PMID:32559632
Abstract
摘要

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