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Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”
Author(s) -
De la CasaFages Beatriz,
FernándezEulate Gorka,
Gamez Josep,
BarahonaHernando Raúl,
Morís Germán,
GarcíaBarcina María,
Infante Jon,
Zulaica Miren,
FernándezPelayo Uxoa,
MuñozOreja Mikel,
Urtasun Miguel,
Olaskoaga Ander,
Zelaya Victoria,
Jericó Ivonne,
SaezVillaverde Raquel,
Catalina Irene,
Sola Emma,
MartínezSáez Elena,
Pujol Aurora,
Ruiz Montserrat,
Schlüter Agatha,
Spinazzola Antonella,
MuñozBlanco Jose Luis,
Grandas Francisco,
Holt Ian,
Álvarez Victoria,
López de Munaín Adolfo
Publication year - 2019
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.27899
Subject(s) - general hospital , medicine , humanities , family medicine , art