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Unique C1 inhibitor dysfunction in a kindred without angioedema. I. A mutant C1 INH that inhibits C1-s but not C1-r

Autor: J J Wisnieski, T C Knauss, I Yike, D G Dearborn, R L Narvy, G B Naff

Publikováno v: The Journal of Immunology. 152:3199-3209

We have described hereditary incomplete deficiency of the fourth component of complement (C4) in 10 members of a large kindred. C4 deficiency in this kindred is not linked to C4 loci in the HLA region. C4 synthesis is decreased, and C4 catabolism is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::53e42a2a35861a9e9e201366b33dd8ed
https://doi.org/10.4049/jimmunol.152.6.3199

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Unique C1 inhibitor dysfunction in a kindred without angioedema. I. A mutant C1 INH that inhibits C1-s but not C1-r

Autor: J J, Wisnieski, T C, Knauss, I, Yike, D G, Dearborn, R L, Narvy, G B, Naff

Publikováno v: Journal of immunology (Baltimore, Md. : 1950). 152(6)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1ff63102d90a043b5eff32f4ca280639
https://pubmed.ncbi.nlm.nih.gov/8144914

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