ArticleThe Journal of clinical investigation1992

A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.

P G Gallagher et al.PubMed ↗Full text ↗Publisher ↗

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