Bennett. (2000) Short-chain hydroxyacyl–coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study. The Journal of Pediatrics 137 , 257-259 /TREACEY E.P., LAMBERT D.M., BARNES R. - Short-chain hydroxyacyl-coenzyme. A dehydrogenase deficiency presenting as ...
dehydrogenase and enoyl-CoA hydratase activities. Mutations in this gene result in trifunctional protein deficiency or LCHAD deficiency. The genes of the alpha and beta subunits of the mitochondrial trifunctional protein are located adjacent to each other in the human genome in a head-to-head ...
英文名:HADH (Hydroxyacyl-coenzyme A Dehydrogenase, Mitochondrial, HAD, HADH1, HADHSC, HHF4, M/SCHAD, MGC8392, SCHAD) (MaxLight 490) 中文名: CBNumber:CB04965130 分子式: 分子量:0 MOL File:Mol file HADH (Hydroxyacyl-coenzyme A Dehydrogenase, Mitochondrial, HAD, HADH1, HADHSC, HHF4, M/...
Recombinant Human Hydroxyacyl-Coenzyme A Dehydrogenase 供应商 ProSpec 产品货号 ENZ-499 产品报价 ￥询价/1mg ￥25ug ￥5ug 产品说明书 点击查看 购买方式 在线支付宝及网银支付、支票、现金、电汇,或拨打全国免费服务电话4006800868与我们联系. 产品新闻
Hydroxyacyl-coenzyme A dehydrogenase gene, an acyl-coenzyme A thiolase gene, genetically engineered strains and a use thereof 发明人: FengqingWang;DongzhiWei;LiqinXu;HaohaoLiu;XinbinLiu;NenghuiChen 申请人: 申请日期: 2014-12-12 申请公布日期: 2019-07-16 代理机构: Robert L. Stearns;Dickinson Wri...
英文别名: enoyl-CoA hydratase - 3-hydroxyacyl-CoA dehydrogenase - dodecanoyl-coenzyme A delta-isomerase中文名: 中文别名: CBNumber: CB81317752 分子式: 分子量: 0 MOL File: Mol file 化学性质 安全信息 用途 供应商 0 enoyl-CoA hydratase - 3-hydroxyacyl-CoA dehydrogenase - dodecanoyl-coenzyme A ...
中文名称:enoyl-CoA hydratase - 3-hydroxyacyl-CoA dehydrogenase - dodecanoyl-coenzyme A delta-isomerase 中文同义词: 英文名称:enoyl-CoA hydratase - 3-hydroxyacyl-CoA dehydrogenase - dodecanoyl-coenzyme A delta-isomerase 英文同义词:enoyl-CoA hydratase - 3-hydroxyacyl-CoA dehydrogenase - dodecanoyl-coenzyme...
The hydroxyacyl-coenzyme A dehydrogenase gene encodes a protein (i) or (ii) as follows: (i) having an amino acid sequence according to SEQ ID NO 2; (ii) derived by substituting, deleting or inserting one or more amino acids in the amino acid sequence defined by (i) and having the ...
Long-chain 3- hydroxyacyl -coenzyme A dehydrogenase (L-CHAD) deficienc in a patient with the Bannayan -Riley -Ruvalcaba syndrome. Am J Med Genet 1994; 52:97 -102.Fryburg JS, Pelegano JP, Bennett MJ, Bebin EM. Long-chain 3- hydroxyacyl-coenzyme A dehydrogenase (L-CHAD) deficiency in a...
long-chain 3 hydroxyacyl-coenzyme A dehydrogenaseL-CHAD deficiencymacrocephalyMRIlipid myopathyBannayan-Riley-Ruvalcaba syndrome (BRRS) is an autosomal dominant condition of macrocephaly in combination with lipomas/hemangiomas, hypotonia, developmental delay, and a lipid myopathy. The etiology of the ...