Literature DB >> 5505952

[Biochemical studies on inherited disorders of amino acid metabolism in pediatrics].

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Year:  1970        PMID： 5505952

Source DB:  PubMed          Journal:  Z Klin Chem Klin Biochem        ISSN： 0044-2933


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  2 in total

1.  Defective decarboxylase in branched chain ketoacid oxidase multienzyme complex in classic type of maple syrup urine disease.

Authors:  H W Rüdiger; U Langenbeck; M Schulze-Schencking; H W Goedde
Journal:  Humangenetik       Date:  1972

2.  Evaluation of a heterozygote test for maple syrup urine disease in leucocytes and cultured fibroblasts.

Authors:  U Langenbeck; H W Rüdiger; M Schulze-Schencking; W Keller; D Brackertz; H W Goedde
Journal:  Humangenetik       Date:  1971
  2 in total

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