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The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Whole-exome-sequencing-based discovery of human FADD deficiency

Lookup NU author(s): Dr Christopher BaconORCiD, Dr Ki Pang, Professor Andrew Cant, Professor Sophie HambletonORCiD

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Publication metadata

Author(s): Bolze A, Byun M, McDonald D, Morgan NV, Abhyankar A, Premkumar L, Puel A, Bacon CM, Rieux-Laucat F, Pang K, Britland A, Abel L, Cant A, Maher ER, Riedl SJ, Hambleton S, Casanova J-L

Publication type: Article

Publication status: Published

Journal: American Journal of Human Genetics

Year: 2010

Volume: 87

Issue: 6

Pages: 873-881

Print publication date: 25/11/2010

ISSN (print): 0002-9297

ISSN (electronic): 1537-6605

Publisher: Cell Press

URL: http://dx.doi.org/10.1016/j.ajhg.2010.10.028

DOI: 10.1016/j.ajhg.2010.10.028

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Funding

Funder referenceFunder name
Cancer Research Institute
INSERM
Rockefeller University
WellChild foundation
St. Giles Foundation
University Paris Descartes
5UL1RR024143-03Rockefeller University Center for Clinical Translational Science
ANR-08-GENO-015-01ANR
G0701897MRC
R01AA017238

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