Spectrin self-association site: characterization and study of beta-spectrin mutations associated with hereditary elliptocytosis.

Míreanna Comhchosúla

• Spectrin beta-chain variant associated with hereditary elliptocytosis.
  le: Dhermy, D, et al.
  Foilsithe: (1982)
• Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
  le: Tse, W T, et al.
  Foilsithe: (1990)
• Heterogeneous phosphorylation of erythrocyte spectrin beta chain in intact cells.
  le: Pedroni, S, et al.
  Foilsithe: (1993)
• Fast screening methods to detect mutations of spectrin in subjects with hereditary elliptocytosis.
  le: Boulanger, L, et al.
  Foilsithe: (1992)
• Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.
  le: Garbarz, M, et al.
  Foilsithe: (1991)