Simple and rapid detection method for the mutations in SLC22A12 that cause hypouricemia by allele-specific real-time polymerase chain reaction
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference23 articles.
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3. Renal hypouricemia: classification, tubular defect and clinical consequences;Sperling;Contrib Nephrol,1992
4. Acute renal failure with severe loin pain and patchy renal ischemia after anaerobic exercise in patients with or without renal hypouricemia;Ishikawa;Nephron,2002
5. Molecular identification of a renal urate-anion exchanger that regulates blood urate levels;Enomoto;Nature,2002
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1. Low detection limit of uric acid based on Prussian blue-enhanced photothermal effect with microfiber knot resonator;Applied Physics Letters;2024-09-09
2. Hypouricemia: what the practicing rheumatologist should know about this condition;Clinical Rheumatology;2019-10-24
3. Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects;Molecular Genetics & Genomic Medicine;2019-05-26
4. High frequency of SLC22A12 variants causing renal hypouricemia 1 in the Czech and Slovak Roma population; simple and rapid detection method by allele-specific polymerase chain reaction;Urolithiasis;2015-06-02
5. Allele-Specific Real-Time Polymerase Chain Reaction as a Tool for Urate Transporter 1 Mutation Detection;Methods in Molecular Biology;2015
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