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。
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
子内基团(主要为甲基)的变位反应。
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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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diametical, diametral, diametre, diametric, diametrical, diametrically, diamfenetide, diamictite, diamicton, diamide,
相似单词
mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
n. 
位
位Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
丙二酸血症是由于丙二酰
A
位或其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.
位，催化底物分子内团(主要为)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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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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Diana, di-a-naphthythjocarbazone, diancister, diandric, diandrous, diandry, Diane, dianegative, Dianemaceae, dianemycin,
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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变位或其
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
团(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，其表达
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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Dianulitidae, diaoyudaoite, diapason, diapause, diapedesis, diapedetic, diapente, diaper, diaper dermatitis, diaper rash,
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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.
基丙二酸血症是
于基丙二酰辅酶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(主要为基)的变位反应。
声明：以上例
、词性分类
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,
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diaphragmatic hernia, diaphragmatitis, diaphragmatocele, diaphragming, diaphragmless, diaphragm-operated, diaphragm-spot, diaphtherine, diaphthol, diaphthoresis,
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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
。
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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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
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.
变位的辅，催化底物分子内基
(
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，
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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diarrhoea, diarrhoetic, diarsenate, diarsenide, diarsenite, diarsine, diarsonium, diarthrodactylous, diarthrodial, diarthrosis,
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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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diascopy, diasolysis, diasone, diasonograph, diasostic, diasphaltene, diaspicera, diaspirin, diaspironecrobiosis, diaspironecrosis,
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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
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
、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,