Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies.

The first recognized human kindred with hereditary deficiency of the fifth component of complement (C5) is described. The proband, a 20-year-old black female with systemic lupus erythematosus since age 11, lacked serum hemolytic complement activity, even during remission. C5 was undetectable in her...

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Pubblicato in:	J Clin Invest
Autori principali:	Rosenfeld, S I, Kelly, M E, Leddy, J P
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Clinical Investigation 1976
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC436822/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/932197/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI108433
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