COX10/YPL172C Literature Guide Help

Other names published for COX10: YPL172C

COX10 - Disease Gene Related (6)

ReferenceOther Genes Addressed
Khalimonchuk O, et al.  (2012) Oligomerization of heme o synthase in cytochrome oxidase biogenesis is mediated by cytochrome oxidase assembly factor Coa2. J Biol Chem 287(32):26715-26
Moraes CT, et al.  (2004) Defects in the biosynthesis of mitochondrial heme c and heme a in yeast and mammals. Biochim Biophys Acta 1659(2-3):153-9
Steinmetz LM, et al.  (2002) Systematic screen for human disease genes in yeast. Nat Genet 31(4):400-4
Shoubridge EA  (2001) Cytochrome c oxidase deficiency. Am J Med Genet 106(1):46-52
Robinson BH  (2000) Human cytochrome oxidase deficiency. Pediatr Res 48(5):581-5
Valnot I, et al.  (2000) A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency. Hum Mol Genet 9(8):1245-9