Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency.
Boisson, Bertrand
Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency. [electronic resource] - Journal of clinical immunology Jul 2017 - 397-412 p. digital
Publication Type: Journal Article; Review
1573-2592
10.1007/s10875-017-0400-z doi
Alleles
Animals
Enzyme Activation
Gain of Function Mutation
Gene Expression Regulation
Genetic Association Studies
Genetic Predisposition to Disease
Germ-Line Mutation
Hematopoietic Stem Cell Transplantation
Heterozygote
Humans
Immunity--genetics
Immunologic Deficiency Syndromes--diagnosis
NF-KappaB Inhibitor alpha--genetics
Organ Specificity--genetics
Phenotype
Phosphorylation
Proteolysis
Severity of Illness Index
Treatment Outcome
Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency. [electronic resource] - Journal of clinical immunology Jul 2017 - 397-412 p. digital
Publication Type: Journal Article; Review
1573-2592
10.1007/s10875-017-0400-z doi
Alleles
Animals
Enzyme Activation
Gain of Function Mutation
Gene Expression Regulation
Genetic Association Studies
Genetic Predisposition to Disease
Germ-Line Mutation
Hematopoietic Stem Cell Transplantation
Heterozygote
Humans
Immunity--genetics
Immunologic Deficiency Syndromes--diagnosis
NF-KappaB Inhibitor alpha--genetics
Organ Specificity--genetics
Phenotype
Phosphorylation
Proteolysis
Severity of Illness Index
Treatment Outcome