Fast screening methods to detect mutations of spectrin in subjects with hereditary elliptocytosis.

مواد مشابهة

• Spectrin beta-chain variant associated with hereditary elliptocytosis.
  بواسطة: Dhermy, D, وآخرون
  منشور في: (1982)
• Spectrin self-association site: characterization and study of beta-spectrin mutations associated with hereditary elliptocytosis.
  بواسطة: Nicolas, G, وآخرون
  منشور في: (1998)
• Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
  بواسطة: Tse, W T, وآخرون
  منشور في: (1990)
• 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.
  بواسطة: Gallagher, P G, وآخرون
  منشور في: (1992)
• Tryptic digestion of spectrin in variants of hereditary elliptocytosis.
  بواسطة: Coetzer, T, وآخرون
  منشور في: (1981)