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Comment
. 2019 Dec;34(12):1932-1933.
doi: 10.1002/mds.27899.

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

Beatriz De la Casa-Fages  1   2   3 , Gorka Fernández-Eulate  4   5 , Josep Gamez  6   7 , Raúl Barahona-Hernando  1   8   9 , Germán Morís  10   11 , María García-Barcina  12 , Jon Infante  13   14 , Miren Zulaica  5   14 , Uxoa Fernández-Pelayo  5 , Mikel Muñoz-Oreja  5 , Miguel Urtasun  4 , Ander Olaskoaga  15 , Victoria Zelaya  16 , Ivonne Jericó  17 , Raquel Saez-Villaverde  18 , Irene Catalina  1   8 , Emma Sola  19 , Elena Martínez-Sáez  20   21 , Aurora Pujol  22   23   24 , Montserrat Ruiz  22   24 , Agatha Schlüter  22   24 , Antonella Spinazzola  25   26 , Jose Luis Muñoz-Blanco  1   3   8 , Francisco Grandas  1   2   3 , Ian Holt  5   27 , Victoria Álvarez  10   28 , Adolfo López de Munaín  4   5   29
Affiliations
Comment

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

Beatriz De la Casa-Fages et al. Mov Disord. 2019 Dec.
No abstract available

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References

    1. De la Casa-Fages B, Fernandez-Eulate G, Gamez J, et al. Parkinsonism and spastic paraplegia type 7: expanding the spectrum of mitochondrial parkinsonism [published online ahead of print August 21, 2019]. Mov Disord. https://doi.org/10.1002/mds.27812
    1. Keshavan N, Abdenur J, Anderson G, et al. The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency [published online ahead of print August 2019]. Genet Med. https://doi.org/10.1038/s41436-019-0613-z
    1. Fink JK. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms. Acta Neuropathol 2013;126(3):307-328. https://doi.org/10.1007/s00401-013-1115-8
    1. Constantinides VC, Papahatzaki MM, Papadimas GK, et al. Diagnostic accuracy of muscle biopsy and electromyography in 123 patients with neuromuscular disorders. In Vivo 2018;32(6):1647-1652. https://doi.org/10.21873/invivo.11427
    1. Harding AE. Classification of the hereditary ataxias and paraplegias. Lancet 1983;1(8334):1151-1155.

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