Mutations in the mitochondrial complex I assembly factor NDUFAF6 cause isolated bilateral striatal necrosis and progressive dystonia in childhood.

MLA

Baide-Mairena, Heidy, et al. “Mutations in the Mitochondrial Complex I Assembly Factor NDUFAF6 Cause Isolated Bilateral Striatal Necrosis and Progressive Dystonia in Childhood.” Molecular Genetics and Metabolism, vol. 126, no. 3, Mar. 2019, pp. 250–58. EBSCOhost, https://doi.org/10.1016/j.ymgme.2019.01.001.

APA

Baide-Mairena, H., Gaudó, P., Marti-Sánchez, L., Emperador, S., Sánchez-Montanez, A., Alonso-Luengo, O., Correa, M., Grau, A. M., Ortigoza-Escobar, J. D., Artuch, R., Vázquez, E., Del Toro, M., Garrido-Pérez, N., Ruiz-Pesini, E., Montoya, J., Bayona-Bafaluy, M. P., & Pérez-Dueñas, B. (2019). Mutations in the mitochondrial complex I assembly factor NDUFAF6 cause isolated bilateral striatal necrosis and progressive dystonia in childhood. Molecular Genetics and Metabolism, 126(3), 250–258. https://doi.org/10.1016/j.ymgme.2019.01.001

Chicago

Baide-Mairena, Heidy, Paula Gaudó, Laura Marti-Sánchez, Sonia Emperador, Angel Sánchez-Montanez, Olga Alonso-Luengo, Marta Correa, et al. 2019. “Mutations in the Mitochondrial Complex I Assembly Factor NDUFAF6 Cause Isolated Bilateral Striatal Necrosis and Progressive Dystonia in Childhood.” Molecular Genetics and Metabolism 126 (3): 250–58. doi:10.1016/j.ymgme.2019.01.001.