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

Lookup NU author(s): Dr David McDonald, Dr Helen GriffinORCiD, Angela Grainger, Dr Louise Reynard, Professor John LoughlinORCiD, Dr Mauro Santibanez Koref, Professor Sophie HambletonORCiD


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Publication metadata

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

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Immunology: Annual Congress of the British Society for Immunology

Year of Conference: 2011

Pages: 43

ISSN: 0019-2805

Publisher: Wiley-Blackwell Publishing Ltd.


DOI: 10.1111/j.1365-2567.2011.03533.x

Library holdings: Search Newcastle University Library for this item

ISBN: 13652567