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

Citation

Broer, S, Bailey, C, Kowalczuk, S et al 2008, 'Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters', Journal of Clinical Investigation, vol. 118, no. 12, pp. 3881-3892.

Year

2008

Fields of Research

  • Receptors And Membrane Biology
  • Cell Physiology

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