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

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	Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression is licensed under a Creative Commons Attribution International License

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Title: Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression
Creator: Tucker, Elena J.
Creator: Wanschers, Bas F. J.
Creator: Szklarczyk, Radek.
Creator: Mountford, Hayley S.
Creator: Wijeyeratne, Xiaonan W.
Creator: van den Brand, Mariël A. M.
Creator: Leenders, Anne M.
Creator: Rodenburg, Richard J.
Creator: Reljić, Boris.
Creator: Compton, Alison G.
Creator: Frazier, Ann E.
Creator: Bruno, Damien L.
Creator: Christodoulou, John.
Creator: Endo, Hitoshi.
Creator: Ryan, Michael T.
Creator: Nijtmans, Leo G.
Creator: Huynen, Martijn A.
Creator: Thorburn, David R.
Date: 2013
Publisher: Public Library of Science.
Funding: 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

Digital Object ID: http://dx.doi.org/10.1371/journal.pgen.1004034
ISSN: 1553-7390
Format: 15 p. (p. 1 - 15)
Language: en
Rights: Open Access. This article has been reproduced here under the terms of a Creative Commons Attribution License (CC BY 4.0) http://creativecommons.org/licenses/by/4.0
Rights: This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Type: journal article
Source: PLoS Genetics, 9(12, e1004034): 1 - 15