Thompson, K., Mai, N., Oláhová, M., Scialó, F., Formosa, L., Stroud, D., . . . Lightowlers, R. (2018). OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect. Springer.
Chicago-čujuhus (17. p.)Thompson, K., et al. OXA1L Mutations Cause Mitochondrial Encephalopathy and a Combined Oxidative Phosphorylation Defect. Springer, 2018.
MLA-čujuhus (9. p.)Thompson, K., et al. OXA1L Mutations Cause Mitochondrial Encephalopathy and a Combined Oxidative Phosphorylation Defect. Springer, 2018.
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