A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis.

Ítems similars

• Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.
  per: Coetzer, T L, et al.
  Publicat: (1991)
• Tryptic digestion of spectrin in variants of hereditary elliptocytosis.
  per: Coetzer, T, et al.
  Publicat: (1981)
• Defective spectrin dimer-dimer association with hereditary elliptocytosis.
  per: Liu, S C, et al.
  Publicat: (1982)
• Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.
  per: Marchesi, S L, et al.
  Publicat: (1987)
• A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.
  per: Lawler, J, et al.
  Publicat: (1984)