APA
De la Casa-Fages B., Fernández-Eulate G., Gamez J., Barahona-Hernando R., Morís G., García-Barcina M., Infante J., Zulaica M., Fernández-Pelayo U., Muñoz-Oreja M., Urtasun M., Olaskoaga A., Zelaya V., Jericó I., Saez-Villaverde R., Catalina I., Sola E., Martínez-Sáez E., Pujol A., Ruiz M., Schlüter A., Spinazzola A., Muñoz-Blanco J. L., Grandas F., Holt I., Álvarez V. & López de Munaín A. (20200128). Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion". : Movement disorders : official journal of the Movement Disorder Society.
Chicago
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 and López de Munaín Adolfo. 20200128. Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion". : Movement disorders : official journal of the Movement Disorder Society.
Harvard
De la Casa-Fages B., Fernández-Eulate G., Gamez J., Barahona-Hernando R., Morís G., García-Barcina M., Infante J., Zulaica M., Fernández-Pelayo U., Muñoz-Oreja M., Urtasun M., Olaskoaga A., Zelaya V., Jericó I., Saez-Villaverde R., Catalina I., Sola E., Martínez-Sáez E., Pujol A., Ruiz M., Schlüter A., Spinazzola A., Muñoz-Blanco J. L., Grandas F., Holt I., Álvarez V. and López de Munaín A. (20200128). Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion". : Movement disorders : official journal of the Movement Disorder Society.
MLA
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 and López de Munaín Adolfo. Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion". : Movement disorders : official journal of the Movement Disorder Society. 20200128.