mfsd8 Literature

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Gene Literature (1)

XB-GENEPAGE-998875

Papers associated with mfsd8

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	Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis., Stiburkova B, Sebesta I, Ichida K, Nakamura M, Hulkova H, Krylov V, Kryspinova L, Jahnova H., Eur J Hum Genet. October 1, 2013; 21 (10): 1067-73.

Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis., Stiburkova B, Sebesta I, Ichida K, Nakamura M, Hulkova H, Krylov V, Kryspinova L, Jahnova H., Eur J Hum Genet. October 1, 2013; 21 (10): 1067-73.

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