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。
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。
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
遗传性
谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
辅
,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。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
基丙二酸血症是由于
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
基)的
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。
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。
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。
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位酶或其辅酶腺苷钴胺素缺陷所致的一
性
谢
。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
位酶的辅酶,催化底物分子内基团(主要为甲基)的
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。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙症是由于甲基丙
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,催化底物分子内基团(主要为甲基)的变位反应。
声明:以上例、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。
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。
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
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。
:
上例句、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。