[HTML][HTML] A Pathogenic Missense Variant in NFKB1 Causes Common Variable Immunodeficiency Due to Detrimental Protein Damage
M Fliegauf, R Krüger, S Steiner, LG Hanitsch… - Frontiers in …, 2021 - frontiersin.org
In common variable immunodeficiency (CVID), heterozygous damaging NFKB1 variants
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
A Pathogenic Missense Variant in NFKB1 Causes Common Variable Immunodeficiency Due to Detrimental Protein Damage
M Fliegauf, R Krüger, S Steiner… - Frontiers in …, 2021 - pubmed.ncbi.nlm.nih.gov
In common variable immunodeficiency (CVID), heterozygous damaging NFKB1 variants
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
[HTML][HTML] A Pathogenic Missense Variant in NFKB1 Causes Common Variable Immunodeficiency Due to Detrimental Protein Damage
M Fliegauf, R Krüger, S Steiner, LG Hanitsch… - Frontiers in …, 2021 - ncbi.nlm.nih.gov
In common variable immunodeficiency (CVID), heterozygous damaging NFKB1 variants
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
A Pathogenic Missense Variant in NFKB1 Causes Common Variable Immunodeficiency Due to Detrimental Protein Damage
M Fliegauf, R Krüger, S Steiner, LG Hanitsch… - Frontiers in …, 2021 - cir.nii.ac.jp
抄録< jats: p> In common variable immunodeficiency (CVID), heterozygous damaging< jats:
italic> NFKB1</jats: italic> variants represent the most frequent monogenic cause.< jats …
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A Pathogenic Missense Variant in NFKB1 Causes Common Variable Immunodeficiency Due to Detrimental Protein Damage.
M Fliegauf, R Krüger, S Steiner, LG Hanitsch… - Frontiers in …, 2021 - europepmc.org
In common variable immunodeficiency (CVID), heterozygous damaging NFKB1 variants
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
A Pathogenic Missense Variant in NFKB1 Causes Common Variable Immunodeficiency Due to Detrimental Protein Damage.
M Fliegauf, R Krüger, S Steiner, LG Hanitsch… - Frontiers in …, 2021 - europepmc.org
In common variable immunodeficiency (CVID), heterozygous damaging NFKB1 variants
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …
represent the most frequent monogenic cause. NFKB1 encodes the precursor p105, which …