异丁酰辅酶A脱氢酶缺乏(Deficiency of isobutyryl-CoA dehydrogenase)基因检测就是线粒体基因检测吗? 是的,异丁酰辅酶A脱氢酶缺乏是一种线粒体基因突变导致的遗传疾病,因此基因检测可以通过检测线粒体基因来确定是否存在该疾病。 异丁酰辅酶A脱氢酶缺乏(Deficiency of isobutyryl-CoA dehydrogenase)的有效治好性治疗会...
英文别名: ACAD8 (ARC42, IBD, Isobutyryl-CoA Dehydrogenase, Mitochondrial, Activator-recruited Cofactor 42kD Component, Acyl-CoA Dehydrogenase Family Member 8, ACAD-8, FLJ22590) (MaxLight 650)中文名: 中文别名: CBNumber: CB04959519 分子式: 分子量: 0 ...
Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism. Molecular Genetics and Metabolism . 1998; 65 (4):264–... RCA Edu,SD Cederbaum,DS Roe,... 被引量: 0发表: 0年 An Investigation of the Metabolism of Valine to Isobutyl Alcohol in Saccharomyces...