Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.

Podobne zapisy

• Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.
  od: Lane, P A, i wsp.
  Wydane: (1987)
• Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.
  od: Gallagher, P. G., i wsp.
  Wydane: (1996)
• Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
  od: Sahr, K E, i wsp.
  Wydane: (1989)
• Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations.
  od: Marchesi, S L, i wsp.
  Wydane: (1990)
• A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis.
  od: Hassoun, H, i wsp.
  Wydane: (1994)