Spectrin self-association site: characterization and study of beta-spectrin mutations associated with hereditary elliptocytosis.

Most of hereditary elliptocytosis (HE) cases are related to a spectrin dimer (SpD) self-association defect. The severity of haemolysis is correlated with the extent of the SpD self-association defect, which itself depends on the location of the mutation regarding the tetramerization site. This site...

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Détails bibliographiques
Auteurs principaux: Nicolas, G, Pedroni, S, Fournier, C, Gautero, H, Craescu, C, Dhermy, D, Lecomte, M C
Format: Artigo
Langue:Inglês
Publié: 1998
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1219454/
https://ncbi.nlm.nih.gov/pubmed/9576854
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