Whole-exome deep sequencing identifies a novel causative mutation in primary immunodeficiency (2011)

Author(s): McDonald D, Morgan N, Griffin H, Dang TS, Grainger A, Reynard L, Loughlin J, Santibanez-Koref M, Hambleton S

      • Date: 5-8 December 2011
      • Conference Name: Immunology: Annual Congress of the British Society for Immunology
      • Volume: 135 (s1)
      • Pages: 43
      • Publisher: Wiley-Blackwell Publishing Ltd.
      • Publication type: Conference Proceedings (inc. abstract)
      • Bibliographic status: Published



      Angela Grainger
      Research Technician