Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia

ATP13A2 mutations have been implicated in juvenile parkinsonism (PARK9) and neuronal ceroid lipofuscinosis [1]. Recently, association with complicated hereditary spastic paraplegia (HSP) and an amyotrophic lateral sclerosis-like phenotype have been reported. Fil: Miranda, Marcelo Fabian. Clinica Las...

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Bibliographic Details
Published in:Parkinsonism & Related Disorders
Main Authors: Miranda, Marcelo Fabian, Harmuth, Florian, Bustamante, M. Leonor, Rossi, Malco Damian, Sturm, Marc, Magnusson, Ólafur Th, Bauer, Peter, Klockgether, Thomas, Ramirez, Alfredo
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier
Subjects:
ATP13A2
KUFOR-RAKEB SYNDROME
PARKINSONISM
SPG78
https://purl.org/becyt/ford/3.2
https://purl.org/becyt/ford/3
Argentina
Sturm
Ramirez
Islandia
Online Access:http://hdl.handle.net/11336/211363

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