Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.

An abnormal spectrin, in which one subunit is truncated, has been detected in a large German family. The inheritance is autosomal dominant. The affected members of the family suffer in widely varying degree from a microcytic hemolytic anemia. The red cell morphology varies correspondingly from smoot...

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Dades bibliogràfiques

Publicat a:	J Clin Invest
Autors principals:	Eber, S W, Morris, S A, Schröter, W, Gratzer, W B
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Clinical Investigation 1988
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC329600/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3276733/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113350
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