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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Dades bibliogràfiques

Publicat a:	J Clin Invest
Autors principals:	Rosenfeld, S I, Kelly, M E, Leddy, J P
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Clinical Investigation 1976
Matèries:	Research Article
Accés en línia:	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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