Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”

Volume: 34, Issue: 12, Pages: 1932 - 1933
Published: Dec 1, 2019
Abstract
Movement DisordersVolume 34, Issue 12 p. 1932-1933 Letters: Published Articles Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion” Beatriz De la Casa-Fages MD, PhD, Beatriz De la Casa-Fages MD, PhD orcid.org/0000-0003-0486-3308 Department of Neurology, Hospital General Universitario Gregorio Marañon, Madrid, Spain Movement Disorders Unit, National Referral Center for Rare Diseases with Movement...
Paper Details
Title
Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”
Published Date
Dec 1, 2019
Volume
34
Issue
12
Pages
1932 - 1933
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