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González-Quintana A, García-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

González-Quintana, Adrián, Inés García-Consuegra, Amaya Belanger-Quintana, Pablo Serrano-Lorenzo, Alejandro Lucia, Alberto Blázquez, Jorge Docampo, Cristina Ugalde, María Morán, Joaquín 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

González-Quintana, A., García-Consuegra, I., Belanger-Quintana, A., Serrano-Lorenzo, P., Lucia, A., Blázquez, A., Docampo, J., Ugalde, C., Morán, M., Arenas, J., & Martín, 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