A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease
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| Description | scientific article |
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author: Brigitte Meunier Maria Bitner-Glindzicz Shamima Rahman Michael I Sadowski Andrew Singleton John Anthony Hardy Luis C. López |
| Publication date | May 2009 |
| Language | English |
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