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

Benzer Materyaller

• Spectrin beta-chain variant associated with hereditary elliptocytosis.
  Yazar:: Dhermy, D, ve diğerleri
  Baskı/Yayın Bilgisi: (1982)
• Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
  Yazar:: Tse, W T, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• Heterogeneous phosphorylation of erythrocyte spectrin beta chain in intact cells.
  Yazar:: Pedroni, S, ve diğerleri
  Baskı/Yayın Bilgisi: (1993)
• Fast screening methods to detect mutations of spectrin in subjects with hereditary elliptocytosis.
  Yazar:: Boulanger, L, ve diğerleri
  Baskı/Yayın Bilgisi: (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.
  Yazar:: Garbarz, M, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)