Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference22 articles.
1. Molecular identification of a renal urate-anion exchanger that regulates blood urate levels;Enomoto;Nature,2002
2. Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia;Matsuo;Am J Hum Genet,2008
3. Hereditary renal hypouricemia: a new Role for allopurinol?;Bhasin;J Am Med,2014
4. Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion;Ichida;J Am Soc Nephrol,2004
5. A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese;Iwai;Kidney Int,2004
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