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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Detalles Bibliográficos

Publicado en:	J Clin Invest
Principais autores:	Rosenfeld, S I, Kelly, M E, Leddy, J P
Formato:	Artigo
Idioma:	Inglês
Publicado:	American Society for Clinical Investigation 1976
Assuntos:	Research Article
Acceso en liña:	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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