Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.

The interaction of spectrin with spectrin-depleted inside-out membrane vesicles was studied in a kindred with an atypical variant of hereditary elliptocytosis inherited in a recessive manner. The probands are characterized by prominent elliptocytosis, decreased erythrocyte thermal stability, an alte...

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Dades bibliogràfiques

Publicat a:	J Clin Invest
Autors principals:	Zail, S S, Coetzer, T L
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Clinical Investigation 1984
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC425229/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6236232/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111491
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