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Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2 by Dinour, D.; Gray, N. K.; Ganon, L.; Knox, A. J. S.; Shalev, H.; Sela, B.-A.; Campbell, S.; Sawyer, L.; Shu, X.; Valsamidou, E.; Landau, D.; Wright, A. F.; Holtzman, E. J. is a Medicine article available to read on EtoBox.

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Author
Dinour, D.; Gray, N. K.; Ganon, L.; Knox, A. J. S.; Shalev, H.; Sela, B.-A.; Campbell, S.; Sawyer, L.; Shu, X.; Valsamidou, E.; Landau, D.; Wright, A. F.; Holtzman, E. J.
Publisher
Oxford University Press; Oxford University Press (OUP) (ISSN 0931-0509)
Published
2011
Field
Medicine (Health Sciences)

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Browse all works by Dinour, D.; Gray, N. K.; Ganon, L.; Knox, A. J. S.; Shalev, H.; Sela, B.-A.; Campbell, S.; Sawyer, L.; Shu, X.; Valsamidou, E.; Landau, D.; Wright, A. F.; Holtzman, E. J.