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Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome.
Rossanti, Rini; Shono, Akemi; Miura, Kenichiro; Hattori, Motoshi; Yamamura, Tomohiko; Nakanishi, Keita; Minamikawa, Shogo; Fujimura, Junya; Horinouchi, Tomoko; Nagano, China; Sakakibara, Nana; Kaito, Hiroshi; Nagase, Hiroaki; Morisada, Naoya; Asanuma, Katsuhiko; Matsuo, Masafumi; Nozu, Kandai; Iijima, Kazumoto.
Afiliação
  • Rossanti R; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Shono A; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Miura K; Department of Pediatric Nephrology, School of Medicine, Tokyo Women's Medical University, Tokyo, Japan.
  • Hattori M; Department of Pediatric Nephrology, School of Medicine, Tokyo Women's Medical University, Tokyo, Japan.
  • Yamamura T; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Nakanishi K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Minamikawa S; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Fujimura J; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Horinouchi T; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Nagano C; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Sakakibara N; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Kaito H; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Nagase H; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Morisada N; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Asanuma K; Department of Nephrology, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Matsuo M; Research Center for Locomotion Biology, Kobe Gakuin University, Kobe, Japan.
  • Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan. nozu@med.kobe-u.ac.jp.
  • Iijima K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
J Hum Genet ; 64(7): 673-679, 2019 Jul.
Article em En | MEDLINE | ID: mdl-31015583
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulosclerose Segmentar e Focal / Complexo de Proteínas Formadoras de Poros Nucleares / Mutação / Síndrome Nefrótica Tipo de estudo: Etiology_studies Limite: Child / Humans / Male Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Japão
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulosclerose Segmentar e Focal / Complexo de Proteínas Formadoras de Poros Nucleares / Mutação / Síndrome Nefrótica Tipo de estudo: Etiology_studies Limite: Child / Humans / Male Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Japão