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Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency.
Elgizouli, M; Lowe, D M; Speckmann, C; Schubert, D; Hülsdünker, J; Eskandarian, Z; Dudek, A; Schmitt-Graeff, A; Wanders, J; Jørgensen, S F; Fevang, B; Salzer, U; Nieters, A; Burns, S; Grimbacher, B.
Afiliación
  • Elgizouli M; Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany.
  • Lowe DM; Faculty of Biology, Albert Ludwigs University, Freiburg, Germany.
  • Speckmann C; Institute of Immunity and Transplantation, University College London, London, UK.
  • Schubert D; Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany.
  • Hülsdünker J; Department of Pediatrics and Adolescent Medicine, University Medical Center, Freiburg, Germany.
  • Eskandarian Z; Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany.
  • Dudek A; Spemann Graduate School of Biology and Medicine (SGBM), Albert Ludwigs University, Freiburg, Germany.
  • Schmitt-Graeff A; Faculty of Biology, Albert Ludwigs University, Freiburg, Germany.
  • Wanders J; Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany.
  • Jørgensen SF; Spemann Graduate School of Biology and Medicine (SGBM), Albert Ludwigs University, Freiburg, Germany.
  • Fevang B; Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany.
  • Salzer U; Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany.
  • Nieters A; Spemann Graduate School of Biology and Medicine (SGBM), Albert Ludwigs University, Freiburg, Germany.
  • Burns S; Department of Pathology, University Medical Center, Freiburg, Germany.
  • Grimbacher B; Institute of Immunity and Transplantation, University College London, London, UK.
Clin Exp Immunol ; 183(2): 221-9, 2016 Feb.
Article en En | MEDLINE | ID: mdl-26437962

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Inmunodeficiencia Variable Común / Fosfatidilinositol 3-Quinasa Clase I / Síndromes de Inmunodeficiencia / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Exp Immunol Año: 2016 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Inmunodeficiencia Variable Común / Fosfatidilinositol 3-Quinasa Clase I / Síndromes de Inmunodeficiencia / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Exp Immunol Año: 2016 Tipo del documento: Article País de afiliación: Alemania