Literature DB >> 782454

The implications of multiple forms of phenylalanine hydroxylase in phenylketonuria and related diseases of phenylalanine metabolism.

J A Barranger.   

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Year:  1976        PMID： 782454     DOI： 10.1016/0006-2944(76)90074-0

Source DB:  PubMed          Journal:  Biochem Med        ISSN： 0006-2944


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  4 in total

1.  Phenylketonuria and its variants.

Authors:  L I Woolf
Journal:  West J Med       Date:  1979-10

2.  Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria.

Authors:  K H Choo; R G Cotton; D M Danks; I G Jennings
Journal:  Biochem J       Date:  1979-08-01       Impact factor: 3.857

3.  Urinary excretion of aromatic acids in hyperphenylalaninemic states: response to a protein challenge.

Authors:  P Koepp; M Scholtyssek; C Plettner
Journal:  Eur J Pediatr       Date:  1978-04-20       Impact factor: 3.183

Review 4.  Diseases of phenylalanine metabolism.

Authors:  C E Parker
Journal:  West J Med       Date:  1979-10
  4 in total

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