Literature DB >> 5582930

The enzyme defect in maple syrup urine disease (branched chain ketoaciduria).

J E Seegmiller, R G Westall.   

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Year:  1967        PMID： 5582930     DOI： 10.1111/j.1365-2788.1967.tb00233.x

Source DB:  PubMed          Journal:  J Ment Defic Res        ISSN： 0022-264X


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  3 in total

1.  Maple syrup urine disease: branched-chain keto acid decarboxylation in fibroblasts as measured with amino acids and keto acids.

Authors:  J Dancis; J Hutzler; R P Cox
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

2.  Maple syrup urine disease: branched-chain amino acid concentrations and metabolism in cultured human lymphoblasts.

Authors:  S D Skaper; D P Molden; J E Seegmiller
Journal:  Biochem Genet       Date:  1976-08       Impact factor: 1.890

3.  Activities of branched-chain 2-oxo acid dehydrogenase and its components in skin fibroblasts from normal and classical-maple-syrup-urine-disease subjects.

Authors:  D T Chuang; W L Niu; R P Cox
Journal:  Biochem J       Date:  1981-10-15       Impact factor: 3.857
  3 in total

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