✦ LIBER ✦
A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease
✍ Scribed by Andrew J. Duncan; Maria Bitner-Glindzicz; Brigitte Meunier; Harry Costello; Iain P. Hargreaves; Luis C. López; Michio Hirano; Catarina M. Quinzii; Michael I. Sadowski; John Hardy; Andrew Singleton; Peter T. Clayton; Shamima Rahman
- Book ID
- 113422631
- Publisher
- American Society of Human Genetics
- Year
- 2009
- Tongue
- English
- Weight
- 487 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0002-9297
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