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Autosomal recessive combines immunodeficiency due to loss of function mutation in Tripeptidyl Peptidase II

Lookup NU author(s): Professor Sophie HambletonORCiD, Dr David McDonald, Dr Helen GriffinORCiD, Angela Grainger, Dr Louise Reynard, Professor Andrew GenneryORCiD, Professor Mary Slatter, Dr Terence Flood, Dr Mario Abinun, Professor John LoughlinORCiD, Professor Jeremy LakeyORCiD, Professor Andrew Cant, Dr Mauro Santibanez Koref


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Publication metadata

Author(s): Hambleton S, McDonald DO, Morgan NV, Griffin H, Singh-Dang T, Grainger A, Reynard L, Gennery AR, Slatter M, Flood TJ, McKiernan P, Barge D, Abinun M, Hackett S, Loughlin J, Lakey J, Cant AJ, Santibanez-Koref M

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: 15th Biennial Meeting European Society for Immunodeficiency (ESID)

Year of Conference: 2012

Pages: 384-385

ISSN: 0271-9142

Publisher: Springer


DOI: 10.1007/s10875-012-9756-2

Library holdings: Search Newcastle University Library for this item

Series Title: Journal of Clinical Immunology

ISBN: 15732592