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

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Bibliographic Details
Published in:Movement disorders 2019-12, Vol.34 (12), p.1932-1933
Main Authors: De la Casa‐Fages, Beatriz, Fernández‐Eulate, Gorka, Gamez, Josep, Barahona‐Hernando, Raúl, Morís, Germán, García‐Barcina, María, Infante, Jon, Zulaica, Miren, Fernández‐Pelayo, Uxoa, Muñoz‐Oreja, Mikel, Urtasun, Miguel, Olaskoaga, Ander, Zelaya, Victoria, Jericó, Ivonne, Saez‐Villaverde, Raquel, Catalina, Irene, Sola, Emma, Martínez‐Sáez, Elena, Pujol, Aurora, Ruiz, Montserrat, Schlüter, Agatha, Spinazzola, Antonella, Muñoz‐Blanco, Jose Luis, Grandas, Francisco, Holt, Ian, Álvarez, Victoria, López de Munaín, Adolfo
Format: Article
Language:English
Subjects:
ATPases Associated with Diverse Cellular Activities
Basal ganglia
Brain diseases
Central nervous system diseases
DNA, Mitochondrial
Humans
Metalloendopeptidases
Mitochondria
Mitochondrial DNA
Movement disorders
Paraplegia
Parkinsonian Disorders
Spastic Paraplegia, Hereditary
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ISSN:0885-3185
1531-8257
DOI:10.1002/mds.27899