An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect
- 1 October 2012
- journal article
- research article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 91 (4) , 737-743
Abstract
No abstract availableKeywords
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