Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion". (2019)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/mds.27899
PubMed Identifier: 31845766
Publication URI: http://europepmc.org/abstract/MED/31845766
Type: Journal Article/Review
Volume: 34
Parent Publication: Movement disorders : official journal of the Movement Disorder Society
Issue: 12
ISSN: 0885-3185