Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression

Elena J. Tucker, Bas F J Wanschers, Radek Szklarczyk, Hayley S. Mountford, Xiaonan W. Wijeyeratne, Mariel A. M. van den Brand, Anne M. Leenders, Richard J Rodenburg, Boris Reljic, Alison G. Compton, Ann E. Frazier, Damien L. Bruno, John Christodoulou, Hitoshi Endo, Michael T. Ryan, Leo G Nijtmans, Martijn A Huynen, David R. Thorburn

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Article numbere1004034
JournalPlos Genetics
Volume9
Issue number12
DOIs
Publication statusPublished - Dec 2013

Cite this

Tucker, E. J., Wanschers, B. F. J., Szklarczyk, R., Mountford, H. S., Wijeyeratne, X. W., van den Brand, M. A. M., Leenders, A. M., Rodenburg, R. J., Reljic, B., Compton, A. G., Frazier, A. E., Bruno, D. L., Christodoulou, J., Endo, H., Ryan, M. T., Nijtmans, L. G., Huynen, M. A., & Thorburn, D. R. (2013). Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression. Plos Genetics, 9(12), [e1004034]. https://doi.org/10.1371/journal.pgen.1004034