Jarolim P.,1995
Jarolim P., Rubin H.L., Brabec V., Palec J. A nonsense mutation glu1669-to-ter within the regulatory domain of human reythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis. - J.Clin.Invest., 1995, v. 95, p. 941-947.
Смотрите также:
