Tucker, E. J., Wanschers, B. F. J., Szklarczyk, R., Mountford, H. S., Wijeyeratne, X. W., van den Brand, M. A. M., . . . Thorburn, D. R. (2013). Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression. Public Library of Science.
Citação norma ChicagoTucker, Elena J., et al. Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated With Perturbed Cytochrome B Protein Expression. Public Library of Science, 2013.
MLA CitationTucker, Elena J., et al. Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated With Perturbed Cytochrome B Protein Expression. Public Library of Science, 2013.