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Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

  • Stefan Bröer
  • , Charles G. Bailey
  • , Sonja Kowalczuk
  • , Cynthia Ng
  • , Jessica M. Vanslambrouck
  • , Helen Rodgers
  • , Christiane Auray-Blais
  • , Juleen A. Cavanaugh
  • , Angelika Bröer
  • , John E.J. Rasko

    Research output: Contribution to journal › Article › peer-review

    100 Citations (Scopus)

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    Biochemistry, Genetics and Molecular Biology