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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类Cytochrome C species
- 线粒体细胞色素CApoptosis
- 细胞cell
- 细胞色素C氧化酶ICOI
- 细胞色素cytochrome
- 细胞色素Ccytochrome C
- 马心细胞色素CCytochrome C
- 一步法分析细胞色素P450 2D6酶活性缺陷等位基因CYP2D6A和CYP2D6BGenotyping of cytochrome P450 2D6 enzyme deficient alleles CYP2D6A and CYP2D6B by one?step ASA analysis
- 潜细胞色素Ccryptocytochrome C
- 类细胞色素ccytochromoid c
- 细胞色素BC1cytochrome BC1
- 细胞色素3A1CYP3A1
- 色素沉淀细胞色素的下沉Deposition of pigment by cells.
- 细胞色素C前体apocytochromc C
- 类细胞色素 Ccytochromoid C
- 细胞色素b序列cytochromeb sequences
- 细胞色素b基因cytochrome b gene
- 潜细胞色素 Ccryptocytochrome C
- 细胞色素途径Cytochrome pathway
