Toggle Main Menu Toggle Search

Open Access padlockePrints

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

Lookup NU author(s): Dr David McDonald, Dr Helen Griffin, Angela Grainger, Dr Louise Reynard, Professor John Loughlin, Dr Mauro Santibanez Koref, Professor Sophie Hambleton


Full text for this publication is not currently held within this repository. Alternative links are provided below where available.

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


Find at Newcastle University icon    Link to this publication