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Table_1_Common variable immunodeficiency in two kindreds wi..:
Frederik Staels
;
Kerstin De Keukeleere
;
Matias Kinnunen
...
doi:10.3389/fimmu.2022.973543.s010. , 2022
Link:
https://doi.org/10.3389/fimmu.2022.973543.s010
RT Journal T1
Table_1_Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations.docx
UL https://suche.suub.uni-bremen.de/peid=base-ftfrontimediafig:oai:figshare.com:article_21159367&Exemplar=1&LAN=DE A1 Frederik Staels A1 Kerstin De Keukeleere A1 Matias Kinnunen A1 Salla Keskitalo A1 Flaminia Lorenzetti A1 Michiel Vanmeert A1 Teresa Prezzemolo A1 Emanuela Pasciuto A1 Eveline Lescrinier A1 Xavier Bossuyt A1 Margaux Gerbaux A1 Mathijs Willemsen A1 Julika Neumann A1 Sien Van Loo A1 Anniek Corveleyn A1 Karen Willekens A1 Ingeborg Stalmans A1 Isabelle Meyts A1 Adrian Liston A1 Stephanie Humblet-Baron A1 Mikko Seppänen A1 Markku Varjosalo A1 Rik Schrijvers YR 2022 K1 Immunology K1 Applied Immunology (incl. Antibody Engineering K1 Xenotransplantation and T-cell Therapies) K1 Autoimmunity K1 Cellular Immunology K1 Humoural Immunology and Immunochemistry K1 Immunogenetics (incl. Genetic Immunology) K1 Innate Immunity K1 Transplantation Immunology K1 Tumour Immunology K1 Immunology not elsewhere classified K1 Genetic Immunology K1 Animal Immunology K1 Veterinary Immunology K1 primary immunodeficiency K1 functional validation K1 novel mutation K1 Nfkb1 (p50) K1 haploinsufficiency JF doi:10.3389/fimmu.2022.973543.s010 LK http://dx.doi.org/https://doi.org/10.3389/fimmu.2022.973543.s010 DO https://doi.org/10.3389/fimmu.2022.973543.s010 SF ELIB - SuUB Bremen
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