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More severe than CVID: Combined immunodeficiency due to a novel NFKB2 mutation.
Bienias, Marc; Gabrielyan, Anastasia; Geberzahn, Linda; Rösen-Wolff, Angela; Huebner, Angela; Jacobsen, Eva-Maria; Toepfner, Nicole; Fang, Mingyan; Lee-Kirsch, Min Ae; Roesler, Joachim; Schuetz, Catharina.
Afiliación
  • Bienias M; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Gabrielyan A; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Geberzahn L; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Rösen-Wolff A; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Huebner A; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Jacobsen EM; Department of Pediatrics, Ulm University Medical Center, Ulm, Germany.
  • Toepfner N; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Fang M; BGI Genomics, Shenzhen, China.
  • Lee-Kirsch MA; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Roesler J; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Schuetz C; Department of Pediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Pediatr Allergy Immunol ; 32(4): 793-797, 2021 05.
Article en En | MEDLINE | ID: mdl-33369776
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunodeficiencia Variable Común / Enfermedades de Inmunodeficiencia Primaria Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Pediatr Allergy Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA / PEDIATRIA Año: 2021 Tipo del documento: Article País de afiliación: Alemania
Texto completo
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunodeficiencia Variable Común / Enfermedades de Inmunodeficiencia Primaria Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Pediatr Allergy Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA / PEDIATRIA Año: 2021 Tipo del documento: Article País de afiliación: Alemania