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2-Methylacyl-CoA dehydrogenaseNo Abstract available for this chapter.doi:10.1007/978-3-642-58051-2_144Professor Dr. Dietmar SchomburgMargit SalzmannDr. Drte StephanSpringer Berlin Heidelberg
Short-chain 3-hydroxy-2-methylacyl-CoA dehydrogenase from rat liver:purification and characterization of a novel enzyme of isoleucine metabol ism. Luo MJ,Mao LF,Schulz H. Archive of Biochemistry and Biophysics . 1995Luo,M.J., Mao,L.-F. and Schulz,H. (1995) Short-chain 3-hydroxy-2-...
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there a correlation between genotype and phenotype? Hum Mol Genet, 6 (1997), pp. 695-708 View in Scopus Google Scholar Andresen et al., 1994 ...
, et al. ( 2000 ) Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism . Am J Hum Genet...