Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲
酸血症是由于甲酰辅酶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。
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
子内团(主要为甲)的变位反应。
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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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相似单词
mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 变
酶
酶Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲酸血症是由于甲酰辅酶A变
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.
变酶的辅酶，催化底物分子内团(主要为甲)的变
。
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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mycoflora, mycogastritis, mycogenetic, mycogenic, mycogenous, mycogonose, mycogonosis, mycography, mycohaemia, mycohemia,
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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：以上例句、词性分类均由互联网资源自动
，
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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mycophobic, mycophthalmia, mycophthorous, mycophylaxin, Mycophyta, Mycoplana, mycoplankton, mycoplasma, Mycoplasmataceae, Mycoplasmatales,
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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.
甲丙二酸血症是由于甲丙二酰
酶A变位酶
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.
变位酶的酶，催化底物分子内
(
要为甲)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，
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
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲丙二酸血症是由于甲丙二酰
A变位或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.
变位的，催化底物分子
(主要为甲)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，表达
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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myelogram, myelogramme, myelography, myeloid, myeloid leukemia, myeloidin, myeloidosis, myelokentric, myelolymphangioma, myelolymphocyte,
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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辅A变位或其辅腺苷钴胺
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.
变位的辅，
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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myelopathy, myeloperoxidase, myelopetal, myelophthisis, myeloplast, myeloplax, myeloplaxoma, myeloplegia, myelopoiesis, myelopore,
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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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myelosyringosis, myelotome, myelotomy, myelotoxicity, myenteric, myenteric plexus, myenteron, Mygalomorphae, myiasis, myiocephalum,
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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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mylodontes, mylohyoid, mylohyoideus, Mylone, mylonite, mylonitic, mylonitization, mylonitize, Mylopharyngodon, Mymaridae,
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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
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
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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myobactivirus, myoblast, myoblastoma, myoblastomyoma, myobradia, myocardia, myocardial, myocardial infarct, myocardial infarction, myocardiogram,
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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,