Literature DB >> 7334692

Genetic heterogeneity of familial hypouricemia due to isolated renal tubular defect.

T Suzuki, K Kidoguchi, A Hayashi.   

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Year:  1981        PMID： 7334692     DOI： 10.1007/BF01896136

Source DB:  PubMed          Journal:  Jinrui Idengaku Zasshi        ISSN： 0021-5074


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  4 in total

1.  Familial hypouricaemia due to an isolated tubular defect of urate reabsorption.

Authors:  D Barajas de Frutos; B Bravo Mancheño; N Palomino Urda; J Pedrero Vera
Journal:  Pediatr Nephrol       Date:  1993-02       Impact factor: 3.714

2.  Substantial anti-gout effect conferred by common and rare dysfunctional variants of URAT1/SLC22A12.

Authors:  Yu Toyoda; Yusuke Kawamura; Akiyoshi Nakayama; Hirofumi Nakaoka; Toshihide Higashino; Seiko Shimizu; Hiroshi Ooyama; Keito Morimoto; Naohiro Uchida; Ryuichiro Shigesawa; Kenji Takeuchi; Ituro Inoue; Kimiyoshi Ichida; Hiroshi Suzuki; Nariyoshi Shinomiya; Tappei Takada; Hirotaka Matsuo
Journal:  Rheumatology (Oxford)       Date:  2021-11-03       Impact factor: 7.580

Review 3.  Hypouricemia and Urate Transporters.

Authors:  Naoyuki Otani; Motoshi Ouchi; Kazuharu Misawa; Ichiro Hisatome; Naohiko Anzai
Journal:  Biomedicines       Date:  2022-03-11

4.  Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene.

Authors:  Akiyoshi Nakayama; Yusuke Kawamura; Yu Toyoda; Seiko Shimizu; Makoto Kawaguchi; Yuka Aoki; Kenji Takeuchi; Rieko Okada; Yoko Kubo; Toshihiko Imakiire; Satoko Iwasawa; Hiroshi Nakashima; Masashi Tsunoda; Keiichi Ito; Hiroo Kumagai; Tappei Takada; Kimiyoshi Ichida; Nariyoshi Shinomiya; Hirotaka Matsuo
Journal:  Rheumatology (Oxford)       Date:  2022-03-02       Impact factor: 7.580
  4 in total

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