A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease
- Duncan, A.J.
- Bitner-Glindzicz, M.
- Meunier, B.
- Costello, H.
- Hargreaves, I.P.
- López, L.C.
- Hirano, M.
- Quinzii, C.M.
- Sadowski, M.I.
- Hardy, J.
- Singleton, A.
- Clayton, P.T.
- Rahman, S.
ISSN: 0002-9297
Argitalpen urtea: 2009
Alea: 84
Zenbakia: 5
Orrialdeak: 558-566
Mota: Artikulua