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Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene.
Nakano, Kiyoshi; Kubota, Yasuo; Mori, Takayuki; Chiga, Motoko; Mori, Takayasu; Sonoda, Shyunya; Ueda, Daisuke; Asakura, Isao; Ikegaya, Takeshi; Kagawa, Jiro; Uchida, Shinichi; Kubota, Akira.
Affiliation
  • Nakano K; Department of Pediatrics, Fujieda Municipal General Hospital, Fujieda, Japan.
  • Kubota Y; Department of Pediatrics, Fujieda Municipal General Hospital, Fujieda, Japan.
  • Mori T; Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Chiga M; Department of Pediatrics, Fujieda Municipal General Hospital, Fujieda, Japan.
  • Mori T; Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Sonoda S; Department of Nephrology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Ueda D; Department of Nephrology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Asakura I; Department of Pediatrics, Fujieda Municipal General Hospital, Fujieda, Japan.
  • Ikegaya T; Department of Pediatrics, Fujieda Municipal General Hospital, Fujieda, Japan.
  • Kagawa J; Department of Pediatrics, Fujieda Municipal General Hospital, Fujieda, Japan.
  • Uchida S; Department of Pediatrics, Fujieda Municipal General Hospital, Fujieda, Japan.
  • Kubota A; Department of Pediatrics, Fujieda Municipal General Hospital, Fujieda, Japan.
Nephrology (Carlton) ; 25(11): 818-821, 2020 Nov.
Article in En | MEDLINE | ID: mdl-32619053
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Full text: 1 Database: MEDLINE Main subject: Pseudohypoaldosteronism / Cullin Proteins / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant Language: En Year: 2020 Type: Article
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Full text: 1 Database: MEDLINE Main subject: Pseudohypoaldosteronism / Cullin Proteins / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant Language: En Year: 2020 Type: Article