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methylmalonyl-coa mutase 添加释义

网络释义专业释义英英释义

  甲基丙二酰coa变位酶

甲基丙二酰CoA变位酶

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  变位酶

thymalonic acidemia,MMA)是一种常染色体隐性遗传病,主要是由于甲基丙二酰辅酶A变位酶(Methylmalonyl-CoA mutase,MCM)自身缺陷或其辅酶钴胺素(Cobalamin,cbl,VitB12)代谢缺陷,导致甲基丙二酸、3-羟基...

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短语

Methylmalonyl-CoA Mutase Deficiencies 甲基丙二酸辅酶

  • 甲基丙二酰辅酶a变位酶
  • 甲基丙二酰辅酶a变位酶

·2,447,543篇论文数据,部分数据来源于NoteExpress

Methylmalonyl-CoA mutase

  • abstract: Methylmalonyl Coenzyme A mutase, also known as MCM is an enzyme that catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA and it is involved in key metabolic pathways. It requires a vitamin B-derived prosthetic group, adenosylcobalamin, to function.

以上来源于: WordNet

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