Combined Glucosephosphate Isomerase and Glucose-6-Phosphate Dehydrogenase Deficiency of the Erythrocytes: A New Haemolytic Syndrome
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1971.tb07036.x/fullpdf
Reference20 articles.
1. Hereditary Hemolytic Anemia Associated with Glucosephosphate Isomerase (GPI) Deficiency— a New Enzyme Defect of Human Erythrocytes
2. Quantitative eindimensionale dünnschichtchromatographie der erythrozytenphospholipide
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1. Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin;Blood Cells, Molecules, and Diseases;2018-03
2. A New Variant of Glucosephosphate Isomerase Deficiency with Mild Haemolytic Anaemia (GPI-MYTHO);Scandinavian Journal of Haematology;2009-04-24
3. Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcome;Blood Cells, Molecules, and Diseases;2003-05
4. A hypothesis of haemolysis in haemolytic anaemias associated with enzymopathies;Medical Hypotheses;2002-07
5. Inherited Metabolic Myopathy and Hemolysis Due to a Mutation in Aldolase A;New England Journal of Medicine;1996-04-25
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