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.

Benzer Materyaller

• Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.
  Yazar:: Marchesi, S L, ve diğerleri
  Baskı/Yayın Bilgisi: (1987)
• Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.
  Yazar:: Gallagher, P. G., ve diğerleri
  Baskı/Yayın Bilgisi: (1996)
• A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis.
  Yazar:: Hassoun, H, ve diğerleri
  Baskı/Yayın Bilgisi: (1994)
• Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.
  Yazar:: Coetzer, T L, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)
• Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.
  Yazar:: Lane, P A, ve diğerleri
  Baskı/Yayın Bilgisi: (1987)