[HTML][HTML] Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen, S Posadas-Cantera… - Frontiers in …, 2022 - frontiersin.org
Most of the currently known heterozygous pathogenic NFKB1 (Nuclear factor kappa B
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
[PDF][PDF] Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen, S Posadas-Cantera… - 2022 - helda.helsinki.fi
Heterozygous pathogenic sequence variants in NFKB1 have been identified as the most
frequent monogenic cause in common variable immunodeficiency (CVID)-like diseases (1 …
frequent monogenic cause in common variable immunodeficiency (CVID)-like diseases (1 …
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen… - Frontiers in …, 2022 - pubmed.ncbi.nlm.nih.gov
Most of the currently known heterozygous pathogenic NFKB1 (Nuclear factor kappa B
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50.
M Fliegauf, M Kinnunen, S Posadas-Cantera… - Frontiers in …, 2022 - europepmc.org
Most of the currently known heterozygous pathogenic NFKB1 (Nuclear factor kappa B
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
[PDF][PDF] Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen… - Frontiers in …, 2022 - researchportal.helsinki.fi
Heterozygous pathogenic sequence variants in NFKB1 have been identified as the most
frequent monogenic cause in common variable immunodeficiency (CVID)-like diseases (1 …
frequent monogenic cause in common variable immunodeficiency (CVID)-like diseases (1 …
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen… - FRONTIERS IN …, 2022 - biblio.ugent.be
Most of the currently known heterozygous pathogenic NFKB1 (Nuclear factor kappa B
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
[PDF][PDF] Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen, S Posadas-Cantera… - backoffice.biblio.ugent.be
Heterozygous pathogenic sequence variants in NFKB1 have been identified as the most
frequent monogenic cause in common variable immunodeficiency (CVID)-like diseases (1 …
frequent monogenic cause in common variable immunodeficiency (CVID)-like diseases (1 …
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen… - Frontiers in …, 2022 - discovery.ucl.ac.uk
Most of the currently known heterozygous pathogenic NFKB1 (Nuclear factor kappa B
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
[HTML][HTML] Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen, S Posadas-Cantera… - Frontiers in …, 2022 - ncbi.nlm.nih.gov
Most of the currently known heterozygous pathogenic NFKB1 (Nuclear factor kappa B
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
subunit 1) variants comprise deleterious defects such as severe truncations, internal …
[PDF][PDF] Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50
M Fliegauf, M Kinnunen, S Posadas-Cantera… - 2022 - helda.helsinki.fi
Heterozygous pathogenic sequence variants in NFKB1 have been identified as the most
frequent monogenic cause in common variable immunodeficiency (CVID)-like diseases (1 …
frequent monogenic cause in common variable immunodeficiency (CVID)-like diseases (1 …