Molecular abnormality of phosphoglycerate kinase-Uppsala associated with chronic nonspherocytic hemolytic anemia.

Ítems similars

• Use of cultured lymphoblastoid cells for the study of abnormal enzymes: molecular abnormality of a phosphoglycerate kinase variant associated with hemolytic anemia.
  per: Fujii, H, et al.
  Publicat: (1981)
• Characterization of a phosphoglycerate kinase variant associated with hemolytic anemia.
  per: Yoshida, A, et al.
  Publicat: (1974)
• Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia.
  per: Baronciani, L, et al.
  Publicat: (1995)
• Characterization of a phosphoglycerate kinase deficiency variants not associated with hemolytic anemia.
  per: Krietsch, W K, et al.
  Publicat: (1980)
• Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemia.
  per: Baronciani, L, et al.
  Publicat: (1993)