A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease
Open Access
- 15 May 2009
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 84 (5), 558-566
- https://doi.org/10.1016/j.ajhg.2009.03.018
Abstract
No abstract availableKeywords
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