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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Bibliografiske detaljer

Udgivet i:	Proc Natl Acad Sci U S A
Principais autores:	Pangburn, M K, Schreiber, R D, Müller-Eberhard, H J
Format:	Artigo
Sprog:	Inglês
Udgivet:	National Academy of Sciences 1983
Fag:	Research Article
Online adgang:	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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