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- 细胞色素C氧化酶缺乏的Leigh综合征伴SURF1基因纯合突变Cytochrome c oxydase-deficient Leigh syndrome with homozygous mutation in SURF1 gene (Fren)
- 细胞色素C氧化酶ICOI
- 细胞色素C氧化酶缺乏Cytochrome-c oxidase deficiency
- 细胞色素C氧化酶亚基Ⅰcytochrome C oxidase subunit Ⅰgene
- 细胞色素C氧化酶Ⅰ基因CO1 gene
- １８－氧化酶缺乏症18-oxylase deficiency
- 细胞色素C氧化酶亚基1基因cox1 gene
- 细胞色素Ccytochrome C
- 细胞色素C氧化酶亚单位Ⅰ（COⅠ）cytochrome c oxidase subunit Ⅰ (COⅠ )
- 潜细胞色素Ccryptocytochrome C
- 细胞色素C前体apocytochromc C
- 细胞色素氧化酶ⅡCO Ⅱ
- 亚铁细胞色素Cferrocyanide C; ferrocytochrome C
- 细胞色素表氧化酶Cytoehrome P450 expoxygenase
- 高铁细胞色素Cferricytochrome C
- 铜缺乏对乳牛细胞色素氧化酶组化特征的影响Effect of copper deficiency on the histochemical characteristics of cytochrome oxidase in dairy cattle
- 细胞色素C注射液cytochron-Sinjection15
- 细胞色素氧化酶亚基Icytochrome oxidase subunit I
- 细胞色素C还原酶cytochrome C-reductase
- 细胞色素氧化酶基因1CO Ⅰ
