Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans-Reference-Cited by-同舟云学术

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Published:2018-10 Issue:4 Volume:142 Page:1285-1296
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Tuijnenburg Paul,Lango Allen Hana^ORCID,Burns Siobhan O.,Greene Daniel,Jansen Machiel H.,Staples Emily,Stephens Jonathan,Carss Keren J.,Biasci Daniele,Baxendale Helen,Thomas Moira,Chandra Anita,Kiani-Alikhan Sorena,Longhurst Hilary J.,Seneviratne Suranjith L.,Oksenhendler Eric,Simeoni Ilenia,de Bree Godelieve J.,Tool Anton T.J.,van Leeuwen Ester M.M.,Ebberink Eduard H.T.M.,Meijer Alexander B.,Tuna Salih,Whitehorn Deborah,Brown Matthew,Turro Ernest,Thrasher Adrian J.,Smith Kenneth G.C.,Thaventhiran James E.,Kuijpers Taco W.,Adhya Zoe,Alachkar Hana,Anantharachagan Ariharan,Antrobus Richard,Arumugakani Gururaj,Bacchelli Chiara,Baxendale Helen,Bethune Claire,Bibi Shahnaz,Boardman Barbara,Booth Claire,Browning Michael,Brownlie Mary,Burns Siobhan,Chandra Anita,Clifford Hayley,Cooper Nichola,Davies Sophie,Dempster John,Devlin Lisa,Doffinger Rainer,Drewe Elizabeth,Edgar David,Egner William,El-Shanawany Tariq,Gaspar Bobby,Ghurye Rohit,Gilmour Kimberley,Goddard Sarah,Gordins Pavel,Grigoriadou Sofia,Hackett Scott,Hague Rosie,Harper Lorraine,Hayman Grant,Herwadkar Archana,Hughes Stephen,Huissoon Aarnoud,Jolles Stephen,Jones Julie,Kelleher Peter,Klein Nigel,Kuijpers Taco,Kumararatne Dinakantha,Laffan James,Lango Allen Hana,Lear Sara,Longhurst Hilary,Lorenzo Lorena,Maimaris Jesmeen,Manson Ania,McDermott Elizabeth,Millar Hazel,Mistry Anoop,Morrisson Valerie,Murng Sai,Nasir Iman,Nejentsev Sergey,Noorani Sadia,Oksenhendler Eric,Ponsford Mark,Qasim Waseem,Quinn Ellen,Quinti Isabella,Richter Alex,Samarghitean Crina,Sargur Ravishankar,Savic Sinisa,Seneviratne Suranjith,Sewall Carrock,Shackley Fiona,Simeoni Ilenia,Smith Kenneth G.C.,Staples Emily,Stauss Hans,Steele Cathal,Thaventhiran James,Thomas Moira,Thrasher Adrian,Welch Steve,Willcocks Lisa,Workman Sarita,Worth Austen,Yeatman Nigel,Yong Patrick,Ashford Sofie,Bradley John,Fletcher Debra,Hammerton Tracey,James Roger,Kingston Nathalie,Ouwehand Willem,Penkett Christopher,Raymond F Lucy,Stirrups Kathleen,Veltman Marijke,Young Tim,Ashford Sofie,Brown Matthew,Clements-Brod Naomi,Davis John,Dewhurst Eleanor,Erwood Marie,Frary Amy,Linger Rachel,Martin Jennifer,Papadia Sofia,Rehnstrom Karola,Astle William,Attwood Antony,Bleda Marta,Carss Keren,Daugherty Louise,Deevi Sri,Graf Stefan,Greene Daniel,Halmagyi Csaba,Haimel Matthias,Hu Fengyuan,James Roger,Lango Allen Hana,Matser Vera,Meacham Stuart,Megy Karyn,Penkett Christopher,Shamardina Olga,Stirrups Kathleen,Titterton Catherine,Tuna Salih,Turro Ernest,Yu Ping,von Ziegenweldt Julie,Furnell Abigail,Mapeta Rutendo,Simeoni Ilenia,Staines Simon,Stephens Jonathan,Stirrups Kathleen,Whitehorn Deborah,Rayner-Matthews Paula,Watt Christopher

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference62 articles.

1. Primary immunodeficiency diseases. Report of a WHO scientific group;Clin Exp Immunol,1997

2. Infections in 252 patients with common variable immunodeficiency;Oksenhendler;Clin Infect Dis,2008

3. Common variable immunodeficiency: clinical and immunological features of 248 patients;Cunningham-Rundles;Clin Immunol,1999

4. The 2015 IUIS phenotypic classification for primary immunodeficiencies;Bousfiha;J Clin Immunol,2015

5. Primary immunodeficiency diseases: an update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015;Picard;J Clin Immunol,2015

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