Literature DB >> 13987252

[Hereditary enzyme defects of amino acid metabolism].

B S SCHULTZE-JENA.   

Abstract

Keywords:  ALBINISM; ALKAPTONURIA; AMINO ACIDS; AMINO ACIDURIA; MAPLE SYRUP URINE DISEASE; PHENYLKETONURIA; PROTEIN METABOLISM DISORDERS; TRYPTOPHAN; TYROSINE

Mesh：

Substances：

Year:  1962        PMID： 13987252

Source DB:  PubMed          Journal:  Ergeb Inn Med Kinderheilkd        ISSN： 0071-111X


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  1 in total

1.  [Pathophysiological investigations in the suspicion of phenylketonuria in psychic adult patients].

Authors:  H Sokoll
Journal:  Dtsch Z Nervenheilkd       Date:  1966-10-24
  1 in total

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