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Molecular diagnosis of CVID (common variable immunodeficiency) (gene analysis for ICOS, TNFRSF13B, TNFRSF13C, CD19, CD81, CR2, MS4A1, PRKCD, PLCG2, PIK3CD, PIK3R1, IL21, IL21R, NFKB1, NFKB2, LRBA, CTLA4, VAV1, RAC2, BLK, BTK, IGHM, CD79A, CD79B, IGLL1, BLNK, TCF7L1 , CD40LG, CD40, AICDA, UNG, using whole exome sequencing)

  • Center for Primary Immunodeficiencies Ghent, Jeffrey Modell Foundation diagnostic and research center
  • Department of Respiratory Diseases, Department of Pediatrics and Genetics
  • PID research lab (PIRL), UZ Gent - MRBII - Entrance 38
  • Corneel Heymanslaan 10
  • 9000 GENT
  • Director of laboratory : Pr Filomeen HAERYNCK
  • More information
  • Phone : +32 (0)9 332 64 39
  • Additional Phone : -
  • Fax : -
  • Website
  • Contact
Last update: June 2018

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Whole Exome Sequencing (WES)

List of diseases and genes

List of diseases tested (1)
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