Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria.

Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired hemolytic anemia in which the erythrocytes are abnormally sensitive to lysis by complement. A functional deficiency of membrane-associated complement regulators has been demonstrated on PNH erythrocytes. The two factor H-like proteins, the C3b...

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Vydáno v:	Proc Natl Acad Sci U S A
Hlavní autoři:	Pangburn, M K, Schreiber, R D, Müller-Eberhard, H J
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	National Academy of Sciences 1983
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC384270/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6225118/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.80.17.5430
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