The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia-Reference-Cited by-同舟云学术

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The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia

Published:2004-07-01 Issue:7 Volume:19 Page:728-733
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:
Short-container-title:Pediatric Nephrology

Author:

Komoda Fusako,Sekine Takashi,Inatomi Jun,Enomoto Atsushi,Endou Hitoshi,Ota Toshiyuki,Matsuyama Takeshi,Ogata Tsutomu,Ikeda Masahiro,Awazu Midori,Muroya Koji,Kamimaki Isamu,Igarashi Takashi

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-004-1424-1.pdf

Cited by 73 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Plasma and Urinary Metabolomic Analysis of Gout and Asymptomatic Hyperuricemia and Profiling of Potential Biomarkers: A Pilot Study;Biomedicines;2024-01-27

2. New SLC22A12 (URAT1) Variant Associated with Renal Hypouricemia Identified by Whole-Exome Sequencing Analysis and Bioinformatics Predictions;Genes;2023-09-20

3. Plasma and Urinary Metabolomic Analysis of Gout and Asymptomatic Hyperuricemia and Profiling of Potential Biomarkers: A Pilot Study;2023-08-09

4. Pathogenic Variants of SLC22A12 (URAT1) and SLC2A9 (GLUT9) in Spanish Patients with Renal Hypouricemia: Founder Effect of SLC2A9 Variant c.374C>T; p.(T125M);International Journal of Molecular Sciences;2023-05-08

5. U-shaped association of uric acid to overall-cause mortality and its impact on clinical management of hyperuricemia;Redox Biology;2022-05

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