Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.

Míreanna Comhchosúla

• 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.
  le: Marchesi, S L, et al.
  Foilsithe: (1990)
• An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.
  le: Conboy, J G, et al.
  Foilsithe: (1993)
• Molecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeleton.
  le: Conboy, J, et al.
  Foilsithe: (1986)
• Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.
  le: Marchesi, S L, et al.
  Foilsithe: (1987)
• Clinical and molecular genetic analysis of a Chinese family with hereditary elliptocytosis caused by a novel mutation in the EPB41 gene
  le: Cao, Manxiong, et al.
  Foilsithe: (2021)