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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Опубликовано в::	Proc Natl Acad Sci U S A
Главные авторы:	Pangburn, M K, Schreiber, R D, Müller-Eberhard, H J
Формат:	Artigo
Язык:	Inglês
Опубликовано:	National Academy of Sciences 1983
Предметы:	Research Article
Online-ссылка:	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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