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

Podobne zapisy

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