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...
Published in: | Parkinsonism & Related Disorders |
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Main Authors: | , , , , , , , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Elsevier
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Subjects: | |
Online Access: | http://hdl.handle.net/11336/211363 |