Disease on EC 5.4.2.4 - Bisphosphoglycerate mutase
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DISEASE 
TITLE OF PUBLICATION
LINK TO PUBMED
Anemia
Bisphosphoglycerate Mutase Deficiency Protects against Cerebral Malaria and Severe Malaria-Induced Anemia.
Anemia, Hemolytic
[Congenital non-spherocytic hemolytic anemia by 2,3-diphosphoglycerate mutase deficiency of the erythrocytes in early infancy]
Anemia, Hemolytic
[Metabolic aspects of the erythrocytes in a case of congenital non-spherocytic hemolytic anemia with probable of 2,3-diphosphoglyceromutase deficiency]
Anemia, Refractory
[Enzyme deficiencies of blood cells in bone marrow insufficiency (author's transl]
bisphosphoglycerate mutase deficiency
Bisphosphoglycerate Mutase Deficiency Protects against Cerebral Malaria and Severe Malaria-Induced Anemia.
bisphosphoglycerate mutase deficiency
Compound heterozygosity in a complete erythrocyte bisphosphoglycerate mutase deficiency.
bisphosphoglycerate mutase deficiency
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.
bisphosphoglycerate mutase deficiency
Glycerated hemoglobin alpha 2 beta 2(82) (EF6) N-epsilon-glyceryllysine: a new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency.
bisphosphoglycerate mutase deficiency
Glycerated hemoglobin, alpha 2A beta 2(82) (EF6) N epsilon-glyceryllysine. A new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency.
bisphosphoglycerate mutase deficiency
Red cell enzymopathies as a model of inborn errors of metabolism.
bisphosphoglycerate mutase deficiency
[2,3-diphosphoglycerate metabolism and 2,3-diphosphoglycerate mutase deficiency in erythrocytes]
bisphosphoglycerate mutase deficiency
[Congenital non-spherocytic hemolytic anemia by 2,3-diphosphoglycerate mutase deficiency of the erythrocytes in early infancy]
bisphosphoglycerate mutase deficiency
[Diphosphoglyceromutase deficiency: new cases associated with erythrocytosis]
bisphosphoglycerate mutase deficiency
[Familial diphosphoglycerate mutase deficiency: hematological and biochemical study]
bisphosphoglycerate mutase deficiency
[Metabolic aspects of the erythrocytes in a case of congenital non-spherocytic hemolytic anemia with probable of 2,3-diphosphoglyceromutase deficiency]
Leukemia, Erythroblastic, Acute
Molecular cloning and nucleotide sequence of murine 2,3-bisphosphoglycerate mutase cDNA.
Malaria
The use of enzymopathic human red cells in the study of malarial parasite glucose metabolism.
Malaria, Cerebral
Bisphosphoglycerate Mutase Deficiency Protects against Cerebral Malaria and Severe Malaria-Induced Anemia.
Malaria, Falciparum
The use of enzymopathic human red cells in the study of malarial parasite glucose metabolism.
Neoplasms
Phosphoglycerate mutase, 2,3-bisphosphoglycerate phosphatase and enolase activity and isoenzymes in lung, colon and liver carcinomas.
Polycythemia
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.
Polycythemia
Uniparental disomy (UPD) of a novel bisphosphoglycerate mutase (BPGM) mutation leading to erythrocytosis.
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