Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression
Elena J Tucker, Bas FJ Wanschers, Radek Szklarczyk, Hayley S Mountford, Xiaonan W Wijeyeratne, Mariel AM 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
PLOS GENETICS | PUBLIC LIBRARY SCIENCE | Published : 2013
Awarded by Australian National Health and Medical Research Council
Awarded by NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
This work was supported by grants (1023619), a Principal Research Fellowship (D1022896, DRT) and a Peter Doherty Early Career Fellowship (1054432, EJT) from the Australian National Health and Medical Research Council, the Victorian Government's Operational Infrastructure Support Program (DRT), the Netherlands Genomics Initiative (Horizon Programme) and the Centre for Systems Biology and Bioenergetics. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.