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Human disease-related mutations in cytochrome b studied in yeast.
Fisher N, Castleden CK, Bourges I, Brasseur G, Dujardin G, Meunier B. Fisher N, et al. Among authors: meunier b. J Biol Chem. 2004 Mar 26;279(13):12951-8. doi: 10.1074/jbc.M313866200. Epub 2004 Jan 12. J Biol Chem. 2004. PMID: 14718526 Free article.
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
Duncan AJ, Bitner-Glindzicz M, Meunier B, Costello H, Hargreaves IP, López LC, Hirano M, Quinzii CM, Sadowski MI, Hardy J, Singleton A, Clayton PT, Rahman S. Duncan AJ, et al. Among authors: meunier b. Am J Hum Genet. 2009 May;84(5):558-66. doi: 10.1016/j.ajhg.2009.03.018. Epub 2009 Apr 16. Am J Hum Genet. 2009. PMID: 19375058 Free PMC article.
556 results