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A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype.
Oe, Yuji; Mishima, Eikan; Mori, Takayasu; Okamoto, Koji; Honkura, Yohei; Nagasawa, Tasuku; Yoshida, Mai; Sato, Hiroshi; Suzuki, Jun; Ikeda, Ryoukichi; Sohara, Eisei; Uchida, Shinichi; Katori, Yukio; Miyazaki, Mariko.
Afiliación
  • Oe Y; Division of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Graduate School of Medicine, Japan.
  • Mishima E; Department of Community Medical Support, Tohoku Medical Megabank Organization, Tohoku University, Japan.
  • Mori T; Division of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Graduate School of Medicine, Japan.
  • Okamoto K; Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan.
  • Honkura Y; Division of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Graduate School of Medicine, Japan.
  • Nagasawa T; Department of Community Medical Support, Tohoku Medical Megabank Organization, Tohoku University, Japan.
  • Yoshida M; Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan.
  • Sato H; Division of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Graduate School of Medicine, Japan.
  • Suzuki J; Division of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Graduate School of Medicine, Japan.
  • Ikeda R; JR Sendai Hospital, Japan.
  • Sohara E; Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan.
  • Uchida S; Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, Japan.
  • Katori Y; Department of Nephrology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Japan.
  • Miyazaki M; Department of Nephrology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Japan.
Intern Med ; 60(18): 2991-2996, 2021 Sep 15.
Article en En | MEDLINE | ID: mdl-33814499
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glomeruloesclerosis Focal y Segmentaria / Síndrome de la Uña-Rótula / Nefritis Hereditaria Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Aged / Female / Humans Idioma: En Revista: Intern Med Asunto de la revista: MEDICINA INTERNA Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Japón
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glomeruloesclerosis Focal y Segmentaria / Síndrome de la Uña-Rótula / Nefritis Hereditaria Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Aged / Female / Humans Idioma: En Revista: Intern Med Asunto de la revista: MEDICINA INTERNA Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Japón