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

  1. Lookup NU author(s)
  2. Dr David McDonald
  3. Dr Helen Griffin
  4. Angela Grainger
  5. Dr Louise Reynard
  6. Professor John Loughlin
  7. Dr Mauro Santibanez Koref
  8. Professor Sophie Hambleton
Author(s)McDonald D, Morgan N, Griffin H, Dang TS, Grainger A, Reynard L, Loughlin J, Santibanez-Koref M, Hambleton S
Editor(s)
Publication type Conference Proceedings (inc. Abstract)
Conference NameImmunology: Annual Congress of the British Society for Immunology
Conference LocationLiverpool, UK
Year of Conference2011
Legacy Date5-8 December 2011
Volume135 (s1)
Pages43
0019-2805
ISBN13652567
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PublisherWiley-Blackwell Publishing Ltd.
URLhttp://dx.doi.org/10.1111/j.1365-2567.2011.03533.x
DOI10.1111/j.1365-2567.2011.03533.x
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