Isobutyryl-CoA dehydrogenase (IBD) is an enzyme involved in the catabolism of the branched-chain amino acid valine. IBD deficiency is a very rare metabolic disorder, whereby only a few cases have been reported thus far. Recently, we observed a Korean newborn boy with elevated concentration of ...
异丁酰辅酶A脱氢酶缺乏(Deficiency of isobutyryl-CoA dehydrogenase)基因检测致病基因基因鉴定 异丁酰辅酶A脱氢酶缺乏是一种罕见的遗传性疾病,通常由IBD基因的突变引起。进行基因检测可以帮助确定患者是否携带IBD基因的突变,从而确认诊断和制定治疗方案。 基因检测通常通过提取患者的DNA样本,然后对IBD基因进行测序分析,以确...
97.1.9 Isobutyryl-CoA Dehydrogenase Deficiency Of the three mitochondrial dehydrogenases involved in the third step of leucine, isoleucine, and valine metabolism, isobutyryl-CoA dehydrogenase (IBDH) in the valine pathway was the last to be definitively identified (Figure 97-2) (46). As with defic...
英文名称: ACAD8 (ARC42, IBD, Isobutyryl-CoA Dehydrogenase, Mitochondrial, Activator-recruited Cofactor 42kD Component, Acyl-CoA Dehydrogenase Family Member 8, ACAD-8, FLJ22590) (MaxLight 650) 英文同义词: ACAD8 (ARC42, IBD, Isobutyryl-CoA Dehydrogenase, Mitochondrial, Activator-recruited Cofactor ...
ACAD8 (ARC42, IBD, Isobutyryl-CoA Dehydrogenase, Mitochondrial, Activator-recruited Cofactor 42kD Component, Acyl-CoA Dehydrogenase Family Member 8, ACAD-8, FLJ22590) (MaxLight 650)化学性质 安全信息 ACAD8 (ARC42, IBD, Isobutyryl-CoA Dehydrogenase, Mitochondrial, Activator-recruited Cofactor 42kD ...