Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia.

Thalassemic red cells show irregular morphology and maldistribution of glycoproteins and sialic acids. These changes are compatible with damage to the red cell membrane skeleton. To test this possibility, we systematically studied the interconnections of skeletal proteins in patients with a form of...

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Vydáno v:	J Clin Invest
Hlavní autoři:	Shinar, E, Rachmilewitz, E A, Lux, S E
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Clinical Investigation 1989
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC303695/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2521488/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113898
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