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Vanishing urate, acute kidney injury episodes and a homozygous SLC2A9 mutation

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References

  1. Matsuo H, Chiba T, Nagamori S et al (2008) Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia. Am J Hum Genet 83(6):744–751

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  2. Dinour D, Gray NK, Campbell S et al (2010) Homozygous SLC2A9 mutations cause severe renal hypouricemia. J Am Soc Nephrol 21(1):64–72

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  3. Dinour D, Gray NK, Ganon L et al (2012) Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2. Nephrol Dial Transplant 27(3):1035–1041

    Article  CAS  PubMed  Google Scholar 

  4. Enomoto A, Kimura H, Chairoungdua A et al (2002) Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Nature 417(6887):447–452

    CAS  PubMed  Google Scholar 

  5. Ohta T, Sakano T, Igarashi T, Itami N, Ogawa T (2004) Group ARFAwRHR. Exercise-induced acute renal failure associated with renal hypouricaemia: results of a questionnaire-based survey in Japan. Nephrol Dial Transplant 19(6):1447–1453

    Article  PubMed  Google Scholar 

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Authors and Affiliations

  1. Department of Nephrology, Heraklion University Hospital, Heraklion, Crete, Greece

    Ariadni Androvitsanea, Kostas Stylianou, Eleftheria Maragkaki, Michael Tzanakakis, Stavros Stratakis, Ioannis Petrakis & Eugene Daphnis

  2. DNAbiolab, Cretan Centre for Research and Development of Applications on Genetics and Molecular Biology, Heraklion, Greece

    Christophoros Giatzakis

Authors
  1. Ariadni Androvitsanea
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  2. Kostas Stylianou
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  3. Eleftheria Maragkaki
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  4. Michael Tzanakakis
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  5. Stavros Stratakis
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  6. Ioannis Petrakis
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  7. Christophoros Giatzakis
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  8. Eugene Daphnis
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Correspondence to Kostas Stylianou.

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Androvitsanea, A., Stylianou, K., Maragkaki, E. et al. Vanishing urate, acute kidney injury episodes and a homozygous SLC2A9 mutation. Int Urol Nephrol 47, 1035–1036 (2015). https://doi.org/10.1007/s11255-015-1005-1

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  • DOI: https://doi.org/10.1007/s11255-015-1005-1

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