Gallagher P.G.,1992
Gallagher P.G., Tse W.T., Coetzer T., Lecomte M.C., Garbarz M., Zarkowsky H.S., Baruchel A., Ballas S.K., Dhermy D., Palek J., Forget B.G. 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. - J.Clin. Invest.,1992, v. 89, p. 892-898.
