Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span
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Date
Journal Title
Journal ISSN
Volume Title
dc.identifier.issn
dc.identifier.doi
10.1016/j.braindev.2018.02.013
dc.identifier.other
WOS:000433997300003
dc.description.volume
dc.description.issue
Publisher
ELSEVIER SCIENCE BV
DOI
10.1016/j.braindev.2018.02.013
