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1 RBCs) obtained from subjects with homozygous hereditary elliptocytosis.
4 n clinically about the resulting conditions (hereditary elliptocytosis and pyropoikilocytosis), the d
5 membrane, such as hereditary spherocytosis, hereditary elliptocytosis, and hereditary pyropoikilocyt
11 result in a variety of syndromes, including hereditary elliptocytosis (HE), hereditary pyropoikilocy
12 on of spectrin dimers to tetramers result in hereditary elliptocytosis (HE), whereas a deficiency of
13 cell pathologies (hereditary spherocytosis, hereditary elliptocytosis, hereditary hydrocytosis, Sout
14 the tetramer formation site, modeled after a hereditary elliptocytosis mutation in human erythrocyte
15 ss spectrometry characterization of a common hereditary elliptocytosis-related mutation of alpha-spec
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