Published in
Wiley, Movement Disorders, 12(34), p. 1932-1933, 2019
DOI: 10.1002/mds.27899
Links
Tools
Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”
Journal article published in 2019 by
Beatriz De la Casa‐Fages 
,
Gorka Fernández‐Eulate,
Josep Gamez ,
Raúl Barahona‐Hernando,
Germán Morís ,
María García‐Barcina,
Jon Infante,
Miren Zulaica,
Uxoa Fernández‐Pelayo,
Mikel Muñoz‐Oreja,
Miguel Urtasun,
Ander Olaskoaga,
Victoria Zelaya,
Ivonne Jericó,
Raquel Saez‐Villaverde
and other authors.
,
Gorka Fernández‐Eulate,
Josep Gamez ,
Raúl Barahona‐Hernando,
Germán Morís ,
María García‐Barcina,
Jon Infante,
Miren Zulaica,
Uxoa Fernández‐Pelayo,
Mikel Muñoz‐Oreja,
Miguel Urtasun,
Ander Olaskoaga,
Victoria Zelaya,
Ivonne Jericó,
Raquel Saez‐Villaverde
and other authors.
This paper is made freely available by the publisher.
Full text: Download
Preprint: archiving forbidden
Postprint:
archiving forbidden
Published version:
archiving forbidden
Data provided by 