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Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

J Li, WT Lei, P Zhang, F Rapaport… - Journal of Experimental …, 2021 - rupress.org
Autosomal dominant (AD) NFKB1 deficiency is thought to be the most common genetic
etiology of common variable immunodeficiency (CVID). However, the causal link between …
被引用次数：45 相关文章
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[HTML][HTML] Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

J Li, WT Lei, P Zhang, F Rapaport… - Journal of …, 2021 - jglobal.jst.go.jp
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of
common variable immunodeficiency | Article Information | J-GLOBAL Art J-GLOBAL ID:202102222206560769 …

Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.

J Li, WT Lei, P Zhang, F Rapaport… - The Journal of …, 2021 - europepmc.org
Autosomal dominant (AD) NFKB1 deficiency is thought to be the most common genetic
etiology of common variable immunodeficiency (CVID). However, the causal link between …
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[HTML][HTML] Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

J Li, WT Lei, P Zhang, F Rapaport… - The Journal of …, 2021 - ncbi.nlm.nih.gov
Autosomal dominant (AD) NFKB1 deficiency is thought to be the most common genetic
etiology of common variable immunodeficiency (CVID). However, the causal link between …

Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.

J Li, WT Lei, P Zhang… - The Journal of …, 2021 - scholarlyexchange.childrensmercy …
Autosomal dominant (AD) NFKB1 deficiency is thought to be the most common genetic
etiology of common variable immunodeficiency (CVID). However, the causal link between …

Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

J Li, WT Lei, P Zhang, F Rapaport… - The Journal of …, 2021 - pubmed.ncbi.nlm.nih.gov
Autosomal dominant (AD) NFKB1 deficiency is thought to be the most common genetic
etiology of common variable immunodeficiency (CVID). However, the causal link between …