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

First Author  Tucker EJ Year  2013
Journal  PLoS Genet Volume  9
Issue  12 Pages  e1004034
PubMed ID  24385928 Mgi Id 
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Trail: Publication

0 Expression