A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese

NAOHARU IWAI; YUKARI MINO; MAKOTO HOSOYAMADA; NAOMI TAGO; YOSHIHIRO KOKUBO; HITOSHI ENDOU

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A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese

机译：SLC22A12无效导致日本人肾低尿酸血症高发

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A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.BackgroundRecently, SLC22A12 has been identified as a urate-anion exchanger in the human kidney.

机译：日语中由于SLC22A12无效导致肾低尿酸血症的流行率很高。背景技术最近，SLC22A12被确定为人类肾脏中的尿酸阴离子交换剂。

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《Kidney international.》 |2004年第3期|共10页
作者
NAOHARU IWAI; YUKARI MINO; MAKOTO HOSOYAMADA; NAOMI TAGO; YOSHIHIRO KOKUBO; HITOSHI ENDOU;
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中图分类泌尿科学（泌尿生殖系疾病）;
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1. Age and origin of the G774A mutation in SLC22A12 causing renal hypouricemia in Japanese. [J] . Ichida K, Hosoyamada M, Kamatani N, Clinical Genetics: An International Journal of Genetics in Medicine . 2008,第3期

机译：SLC22A12中引起日本人低尿酸血症的G774A突变的年龄和起源。
2. A novel compound heterozygous mutation in the SLC22A12 (URAT1) gene in a Japanese patient associated with renal hypouricemia [J] . Fujita Kyoko, Ichida Kimiyoshi Clinica chimica acta: International journal of clinical chemistry and applied molecular biology . 2016,第Null期

机译：一名日本人与肾脏低尿酸血症有关的SLC22A12（URAT1）基因中的新型复合杂合突变
3. The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia. [J] . Komoda F, Sekine T, Inatomi J, Pediatric nephrology: journal of the International Pediatric Nephrology Association . 2004,第7期

机译：SLC22A12中的W258X突变是日本肾性低尿酸血症的主要原因。
4. Steadily decreasing prevalence of dementia in Japanese urban elderly during a six-year follow-up [C] . Yamamoto C. Hoshi T. International Conference of Alzheimer's Disease International . 2012

机译：在六年的随访期间，稳步下降日本城市老年痴呆症的患病率
5. Association of high-sensitivity cardiac troponin,fibroblast growth factor 23 and left ventricular hypertrophy in Japanese patients with reduced renal function [D] . 伊藤, 敦巳 2019

机译：肾功能减退的日本人高敏感性心肌肌钙蛋白，成纤维细胞生长因子23与左心室肥厚的关系
6. Transplantation of a kidney with a heterozygous mutation in the SLC22A12 (URAT1) gene causing renal hypouricemia: a case report [O] . Kiyokazu Tsuji, Mineaki Kitamura, Kumiko Muta, 2020

机译：用SLC22A12（URAT1）基因的杂合突变移植肾脏突变导致肾低度血症：案例报告
7. A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese [O] . Iwai Naoharu, Mino Yukari, Hosoyamada Makoto, 2004

机译：SLC22A12无效引起的日本人低尿酸血症患病率很高

A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese

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