Glucosephosphate Isomerase (GPI) Deficiency Mutations Associated with Hereditary Nonspherocytic Hemolytic Anemia (HNSHA)

This publication has 23 references indexed in Scilit:

• The Significance of the 187G (H63D) Mutation in Hemochromatosis
  American Journal of Human Genetics, 1997
• The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families
  Blood Cells, Molecules, and Diseases, 1996
• A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
  Nature Genetics, 1996
• Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: Tabulation of mutant enzymes
  American Journal of Hematology, 1996
• Human Glucose Phosphate Isomerase: Exon Mapping and Gene Structure
  Genomics, 1995
• GPI Mount Scopus — a variant of glucosephosphate isomerase deficiency
  Annals of Hematology, 1993
• Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemia.
  Proceedings of the National Academy of Sciences, 1993
• Enzymatic Diagnosis in Non-Spherocytic Hemolytic Anemia
  Medicine, 1988
• Red cell enzyme defects as nondiseases and as diseases
  Blood, 1979
• Glucosephosphate-Isomerase (GPI) Deficiency: GPI Elyria
  Annals of Internal Medicine, 1974