González-Quintana, A.; GarcÃa-Consuegra, I.; Belanger-Quintana, A.; Serrano-Lorenzo, P.; Lucia, A.; Blázquez, A.; Docampo, J.; Ugalde, C.; Morán, M.; Arenas, J.;
et al. Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report. Genes 2020, 11, 855.
https://doi.org/10.3390/genes11080855
AMA Style
González-Quintana A, GarcÃa-Consuegra I, Belanger-Quintana A, Serrano-Lorenzo P, Lucia A, Blázquez A, Docampo J, Ugalde C, Morán M, Arenas J,
et al. Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report. Genes. 2020; 11(8):855.
https://doi.org/10.3390/genes11080855
Chicago/Turabian Style
González-Quintana, Adrián, Inés GarcÃa-Consuegra, Amaya Belanger-Quintana, Pablo Serrano-Lorenzo, Alejandro Lucia, Alberto Blázquez, Jorge Docampo, Cristina Ugalde, MarÃa Morán, JoaquÃn Arenas,
and et al. 2020. "Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report" Genes 11, no. 8: 855.
https://doi.org/10.3390/genes11080855
APA Style
González-Quintana, A., GarcÃa-Consuegra, I., Belanger-Quintana, A., Serrano-Lorenzo, P., Lucia, A., Blázquez, A., Docampo, J., Ugalde, C., Morán, M., Arenas, J., & MartÃn, M. A.
(2020). Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report. Genes, 11(8), 855.
https://doi.org/10.3390/genes11080855