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elliptocytosis
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Tight junction
Homo sapiens (human)
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EPB41
Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability.
Defining of the minimal domain of protein 4.1 involved in spectrin-actin binding.
Cloning and characterization of hdlg: the human homologue of the Drosophila discs large tumor suppressor binds to protein 4.1.
SPTA1
Molecular basis of red cell membrane disorders.
Spectrin-based skeleton in red blood cells and malaria.
Dinucleotide repeat polymorphism at the human erythroid alpha spectrin (SPTA1) locus.
SPTB
Interaction between microtubule-associated protein tau and spectrin
Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis