Articles with public access mandates - Matthew A. Brown - National Institute for Health Research, UKLearn more
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OverallNHMRCNIHMRCNIHRVersus Arthritis, UKWellcomeARCBHFNSFCCIHREuropean CommissionCancer Research UKSwedish Research CouncilGovernment of SpainDFGFWOUK Research & InnovationFRQSGenome CanadaINSERMSNSFHHMISFINWOBBSRCCSOESRCZonMwRCNBMBFHealth Data Research, UKVAEPSRCParkinson's UKANRJDRFMedical Research Future Fund, AustraliaNSFDoDNSERCFraunhofer-GesellschaftDSFMotor Neurone Disease Association, UKDoris Duke Charitable FoundationGovernment of ItalyIFOPADOEGatesNASAFWFDNRFAcademy of FinlandTelethonFORTEKnut and Alice Wallenberg FoundationA*StarBlood Cancer UKDiabetes UKMultiple Sclerosis Society, UKSTFCWorldwide Cancer Research, UKARRSResearch Grants Council, Hong KongMichael J Fox FoundationJST
Available based on mandate: 69
Whole-Genome Sequencing identifies loss-of-function variants in NFKB1 as the most common monogenic cause of Common Variable Immunodeficiency in Europeans
P Tuijnenburg, HL Allen, SO Burns, D Greene, MH Jansen, E Staples, ...
The Journal of allergy and clinical immunology 142 (4), 1285, 2018
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