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FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child.
Rossanti, Rini; Watanabe, Toshio; Nagano, China; Hara, Shigeo; Horinouchi, Tomoko; Yamamura, Tomohiko; Sakakibara, Nana; Ninchoji, Takeshi; Iijima, Kazumoto; Nozu, Kandai.
Afiliação
  • Rossanti R; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan. riniariyadi@gmail.com.
  • Watanabe T; Department of Pediatrics, Fujioka General Hospital, Fujioka, Japan.
  • Nagano C; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.
  • Hara S; Department of Diagnostic Pathology, Kobe City Medical Center General Hospital, Kobe, Japan.
  • Horinouchi T; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.
  • Yamamura T; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.
  • Sakakibara N; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.
  • Ninchoji T; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.
  • Iijima K; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.
  • Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.
CEN Case Rep ; 10(1): 100-105, 2021 02.
Article em En | MEDLINE | ID: mdl-32902815
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteinúria / Caderinas / Glomérulos Renais / Síndrome Nefrótica Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Humans / Male Idioma: En Revista: CEN Case Rep Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteinúria / Caderinas / Glomérulos Renais / Síndrome Nefrótica Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Humans / Male Idioma: En Revista: CEN Case Rep Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão