6. Lee, W. S., & Sokol, R. J. (2013). Mitochondrial hepatopathies: advances in genetics, therapeutic approaches, and outcomes. The Journal of pediatrics, 163(4), 942-948. 7. Nogueira, C., de Souza, C.… Click to show full abstract
6. Lee, W. S., & Sokol, R. J. (2013). Mitochondrial hepatopathies: advances in genetics, therapeutic approaches, and outcomes. The Journal of pediatrics, 163(4), 942-948. 7. Nogueira, C., de Souza, C. F., Husny, A., Derks, T. G., Santorelli, F. M., & Vilarinho, L. (2012). MPV17: fatal hepatocerebral presentation in a Brazilian infant. Molecular genetics and metabolism, 107(4), 764. 8. Sasaki, K., Sakamoto, S., Uchida, H., Narumoto, S., Shigeta, T., Fukuda, A., ... & Kasahara, M. (2017). Liver transplantation for mitochondrial respiratory chain disorder: a single-center experience and excellent marker of differential diagnosis. Transplantation proceedings, (49), 1097-1102. 9. Spinazzola, A., Viscomi, C., Fernandez-Vizarra, E., Carrara, F., D’Adamo, P., Calvo, S., ... & Parini, R. (2006). MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion. Nature genetics, 38(5), 570-575. 10. Vu, T. H., Tanji, K., Holve, S. A., Bonilla, E., Sokol, R. J., Snyder, R. D., ... & De Vivo, D. (2001). Navajo neurohepatopathy: a mitochondrial DNA depletion syndrome?. Hepatology, 34(1), 116-120. P-12.39
               
Click one of the above tabs to view related content.