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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