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August 1, 1979Biochemical JournalOpen Access

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

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Authors

KCK.H. Andy ChooRoyal Children's HospitalRCRichard G.H. CottonMet OfficeDDDavid M. DanksUniversity of San Diego

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Choo et al. (1979) studied this question.

synapsesocial.com/papers/6a87e7b6feba08a241fe7113https://doi.org/10.1042/bj1810285
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1On the Nature of Enzymatic Defect in Phenylpyruvic Oligophrenia1957 · 94 citations
  2. 2Two-dimensional gel electrophoresis of membrane proteins1976 · 699 citations
  3. 3Detection of Hepatic Phenylalanine 4-Hydroxylase in Classical Phenylketonuria1973 · 72 citations
  4. 4The isolation and properties of phenylalanine hydroxylase from rat liver1974 · 69 citations