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

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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

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