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

Published 2020 View Full Article

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Title
Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia
Authors
Keywords
ATP13A2, Kufor-Rakeb syndrome, Spastic paraplegia, SPG78, Parkinsonism
Journal
PARKINSONISM & RELATED DISORDERS
Volume 81, Issue -, Pages 45-47
Publisher
Elsevier BV
Online
2020-10-06
DOI
10.1016/j.parkreldis.2020.10.004
References
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