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Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene
OBJECTIVES: Up to 0.3% of Japanese have hypouricaemia. Most cases appear to result from a hereditary disease, renal hypouricaemia (RHUC), which causes exercise-induced acute kidney injury and urolithiasis. However, to what extent RHUC accounts for hypouricaemia is not known. We therefore investigate...
Autores principales: | Nakayama, Akiyoshi, Kawamura, Yusuke, Toyoda, Yu, Shimizu, Seiko, Kawaguchi, Makoto, Aoki, Yuka, Takeuchi, Kenji, Okada, Rieko, Kubo, Yoko, Imakiire, Toshihiko, Iwasawa, Satoko, Nakashima, Hiroshi, Tsunoda, Masashi, Ito, Keiichi, Kumagai, Hiroo, Takada, Tappei, Ichida, Kimiyoshi, Shinomiya, Nariyoshi, Matsuo, Hirotaka |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889275/ https://www.ncbi.nlm.nih.gov/pubmed/34255816 http://dx.doi.org/10.1093/rheumatology/keab545 |
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