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The Journal of Clinical Investigation|March 1, 1992
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 spectrinP G Gallagher, W T Tse, T Coetzer, et al.
Blood|July 1, 1995
Molecular basis of altered red blood cell membrane properties in Southeast Asian ovalocytosis: role of the mutant band 3 protein in band 3 oligomerization and retention by the membrane skeletonS C Liu, J Palek, S J Yi, et al.
Blood|December 1, 1996
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiencyP Jarolim, J L Murray, H L Rubin, et al.
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