Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression-Reference-Cited by-同舟云学术

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

Published:2013-12-26 Issue:12 Volume:9 Page:e1004034
ISSN:1553-7404
Container-title:PLoS Genetics
language:en
Short-container-title:PLoS Genet

Author:

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

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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