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COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11

Known as: COXPD11, ENCEPHALONEUROMYOPATHY, INFANTILE, DUE TO MITOCHONDRIAL TRANSLATION DEFECT 
National Institutes of Health

Papers overview

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Review
2016
Review
2016
BACKGROUND We report a consanguineous Sudanese family whose two affected sons presented with a lethal disorder characterised by… Expand
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