. . . . . "SPTA1" . . . . "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" . . . . "2018-04-05T10:17:11.353+02:00"^^ . . . . . .