Ataxia and Action Myoclonus Related to Novel Mutations in ATP13A2 Gene

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URI: http://hdl.handle.net/10902/24021
ISSN: 0885-3185
ISSN: 1531-8257
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Autoría
Manrique, Leire; Sánchez-Rodríguez, Antonio; Pelayo Negro, Ana. L.; Corral-Juan, Marc; Matilla-Dueñas, Antoni; Infante Ceberio, JonAutoridad Unican
Fecha
2021-05-19
Derechos
This is the peer reviewed version of the following article: [Manrique, L., Sánchez-Rodríguez, A., Pelayo-Negro, A.L., Corral-Juan, M., Matilla-Dueñas, A. and Infante, J. (2021), Ataxia and Action Myoclonus Related to Novel Mutations in ATP13A2 Gene. Mov Disord Clin Pract, 8: 969-971], which has been published in final form at [https://doi.org/10.1002/mdc3.13260]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Publicado en
Movement Disorders, 2021; Volume8, Issue6; Pages 969-971
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John Wiley and Sons Inc.
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Palabras clave
Ataxia
Myoclonus
ATP13A2
Mutation
Kufor-Rakeb
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