Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review

Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9compound heterozygosity

(2014) Guido Jeannin et al.   BMC Medical Genetics

Hereditary Renal Hypouricemia: A New Role for Allopurinol?

(2013) Bhavna Bhasin et al.   AMERICAN JOURNAL OF MEDICINE

Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis

(2013) Blanka Stiburkova et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Acute kidney injury in two children caused by renal hypouricaemia type 2

(2012) Blanka Stiburkova et al.   PEDIATRIC NEPHROLOGY

Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: Biochemical and molecular genetic analysis in two Czech families with xanthinuria type I

(2011) Blanka Stiburkova et al.   CLINICA CHIMICA ACTA

A case of acute renal failure after exercise with renal hypouricemia demonstrated compound heterozygous mutations of uric acid transporter 1

(2011) Ayami Ochi et al.   Clinical and Experimental Nephrology

Two cases of nephrotic syndrome (NS)-induced acute kidney injury (AKI) associated with renal hypouricemia

(2011) Y. Takeda et al.   CLINICAL NEPHROLOGY

A Case of Exercise-induced Acute Renal Failure with G774A Mutation in SCL22A12 Causing Renal Hypouricemia

(2011) Yong Hyun Kim et al.   JOURNAL OF KOREAN MEDICAL SCIENCE

Novel homozygous insertion in SLC2A9 gene caused renal hypouricemia

(2011) Blanka Stiburkova et al.   MOLECULAR GENETICS AND METABOLISM

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2

(2011) D. Dinour et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Diagnostic Tests for Primary Renal Hypouricemia

(2011) Ivan Sebesta et al.   NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS

Recurrent EIARF and PRES With Severe Renal Hypouricemia by Compound Heterozygous SLC2A9 Mutation

(2011) Y. Shima et al.   PEDIATRICS

Homozygous SLC2A9 Mutations Cause Severe Renal Hypouricemia

(2009) D. Dinour et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Mutations in Glucose Transporter 9 Gene SLC2A9 Cause Renal Hypouricemia

(2008) Hirotaka Matsuo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Plasma Urate Level Is Directly Regulated by a Voltage-driven Urate Efflux Transporter URATv1 (SLC2A9) in Humans

(2008) Naohiko Anzai et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

(2008) Veronique Vitart et al.   NATURE GENETICS