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。
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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、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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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,
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
子内团(主要为甲)的变位反应。
声明：以上例句、词
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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market place, market price, market research, market town, market value, marketability, marketable, marketbasket, marketeer, marketer,
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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
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：
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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mutant, mutant gene, mutants, mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism,
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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
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
基团(主要为甲基)的变位反应。
声明：以上例句、词性类均由互联网资源自动生成，部未经过人工审核，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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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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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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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.
甲丙二酸血症是由于甲丙二
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(主要为甲)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,