Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性
谢疾病。
mutase
/'mjʊtes/ /ˈmjutes/
n. 变位酶
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
变位酶的辅酶，催化底物分子内基团(主要为甲基)的变位反应。
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句、词性分类均由互
源自动生成，部分未经过人工审核，其表达内容亦不
表本软件的观点；若发现问题，欢迎向我们指正。
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chalcogen, chalcogenide, chalcography, chalcolamprite, chalcolite, Chalcolithic, chalcomenite, chalcomorphite, chalcomycin, chalcone,
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 变位
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰
A变位或其腺苷钴胺素
所致的一种遗传性谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
变位的，
化底物分子内基团(主要为甲基)的变位反应。
声明：以上例句、词性分类均由互联网资源自动生成，部分未经过人工审核，其表达内容亦不表本软件的观点；若发现问题，欢迎向我们指正。
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 变位酶
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症
甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
变位酶的辅酶，催化底物分子内基团(主要为甲基)的变位反应。
声
：
例句、词性分类均
互联网资源自动生成，部分未经过人工审核，其表达内容亦不表本软件的观点；若发现问题，欢迎向我们指正。
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chalk out, chalk talk, chalkboard, chalked, chalkiness, chalking, chalklike, chalkogenide, chalkography, chalkostibite,
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 
酶
酶Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙
酸血症是由于甲基丙
酶A
酶或其酶腺苷钴胺素缺陷所致
一种遗传性谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
酶酶，催化底物分子内基团(主要为甲基)反应。
声明：以上例句、词性分类均由互联网资源自动生成，部分未经过人工审核，其表达内容亦不表本软件
观点；若发现问题，欢迎向我们指正。
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 变位酶
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
变位酶的辅酶，催化底物分子内基团(主要为甲基)的变位反应。
声明：以上
、词性分类均
网资源自动生成，部分未经过人工审核，其表达内容亦不表本软件的观点；若发现问题，欢迎向我们指正。
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
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champak, champamycin, champavatin, champers, champertor, champerty, champiaceae, champignon, champion, championship,
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 变位
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰A变位或其腺苷钴胺素缺所
一种遗传性谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
变位，催化底物分子内基团(主要为甲基)变位反应。
声明：以上例句、词性分类均由互联网资源自动生成，部分未经过人工审核，其表达内容亦不表本软件观点；若发现问题，欢迎向我们指正。
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n.
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅A或其辅腺苷钴胺素缺陷所致的一种遗传性谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
的辅，催化底物分子内基团(主要为甲基)的反应。
声明：以上例句、词性分类均由互联网资
生成，部分未经过人工审核，其表达内容亦不表本软件的观点；若发现问题，欢迎向我们指正。
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chancy, Chandar, chandelier, chandelle, Chandigarh, chandler, chandleress, chandlery, chandui, chanduy,
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 变位酶
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗
病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
变位酶的辅酶，催化底物分子内基团(主要为甲基)的变位反应。
声明：以上例句、词
分类均由互联网资源自动生成，部分未经过人工审核，其表达内容亦不表本软件的观点；若发现问题，欢迎向我们指正。
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change up, changeability, changeable, changeableness, changeably, changeabout, changeback, changeful, changeful-gear, changefully,
相似单词
mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 变位酶
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基
血症是由于甲基酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
变位酶的辅酶，催化底物
子内基团(主要为甲基)的变位反应。
声明：以上例句、词
类均由互联网资源自动生成，部未经过人工审核，其表达内容亦不表本软件的观点；若发现问题，欢迎向我们指正。
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,