Your browser doesn't support javascript.
loading
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.
Affiliation
  • 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 in En | MEDLINE | ID: mdl-33369776

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Common Variable Immunodeficiency / Primary Immunodeficiency Diseases Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Pediatr Allergy Immunol Journal subject: ALERGIA E IMUNOLOGIA / PEDIATRIA Year: 2021 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Common Variable Immunodeficiency / Primary Immunodeficiency Diseases Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Pediatr Allergy Immunol Journal subject: ALERGIA E IMUNOLOGIA / PEDIATRIA Year: 2021 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido