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Functional analysis of a novel G87V TNFRSF1A mutation in patients with TNF receptor-associated periodic syndrome.
Tsuji, S; Matsuzaki, H; Iseki, M; Nagasu, A; Hirano, H; Ishihara, K; Ueda, N; Honda, Y; Horiuchi, T; Nishikomori, R; Morita, Y; Mukai, T.
Afiliación
  • Tsuji S; Department of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.
  • Matsuzaki H; Department of Life Sciences, Faculty of Life and Environmental Sciences, Prefectural University of Hiroshima, Shobara, Hiroshima, Japan.
  • Iseki M; Department of Immunology and Molecular Genetics, Kawasaki Medical School, Kurashiki, Okayama, Japan.
  • Nagasu A; Department of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.
  • Hirano H; Department of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.
  • Ishihara K; Department of Immunology and Molecular Genetics, Kawasaki Medical School, Kurashiki, Okayama, Japan.
  • Ueda N; Department of Internal Medicine, Miyazaki Prefectural Miyazaki Hospital, Miyazaki, Japan.
  • Honda Y; Department of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Horiuchi T; Department of Internal Medicine, Kyushu University Beppu Hospital, Beppu, Oita, Japan.
  • Nishikomori R; Department of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Morita Y; Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
  • Mukai T; Department of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.
Clin Exp Immunol ; 198(3): 416-429, 2019 12.
Article en En | MEDLINE | ID: mdl-31429073
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Mutación Missense / Receptores Tipo I de Factores de Necrosis Tumoral / Enfermedades Autoinflamatorias Hereditarias / Fiebre Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male Idioma: En Revista: Clin Exp Immunol Año: 2019 Tipo del documento: Article País de afiliación: Japón
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Mutación Missense / Receptores Tipo I de Factores de Necrosis Tumoral / Enfermedades Autoinflamatorias Hereditarias / Fiebre Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male Idioma: En Revista: Clin Exp Immunol Año: 2019 Tipo del documento: Article País de afiliación: Japón