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Academic Journal

Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression.

  • Authors : Tucker EJ; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia ; Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.

Subjects: Cytochromes b/Cytochromes b/Cytochromes b/*biosynthesis ; Electron Transport Complex III/Electron Transport Complex III/Electron Transport Complex III/*genetics ; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics

  • Source: PLoS genetics [PLoS Genet] 2013; Vol. 9 (12), pp. e1004034. Date of Electronic Publication: 2013 Dec 26.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: Print-Electronic Cited Medium: Internet

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