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C1r deficiency: an inborn error associated with cutaneous and renal disease

The studies of sera from two siblings with C1r deficiency are described. The brother (18 yr old) has shown clinical manifestations resembling lupus erythematosus for 5 yr, and the sister (24 yr old) has had arthralgia and recurrent episodes of rhinobronchitis since early childhood. Three siblings ha...

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Main Authors: Day, N. K., Geiger, H., Stroud, R., deBracco, M., Mancado, B., Windhorst, D., Good, R. A.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 1972
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC292239/
https://ncbi.nlm.nih.gov/pubmed/4623164
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