Phosphoglycerate kinase San Francisco: A new variant associated with hemolytic anemia but not with neuromuscular manifestations
Author:
Publisher
Wiley
Subject
Hematology
Reference27 articles.
1. Complete amino acid sequence of human phosphoglycerate kinase. Cyanogen bromide peptides and complete amino acid sequence.
2. Distribution of genetic variants of erythrocyte phosphoglycerate kinase (PGK) and phosphohexose isomerase (PHI) among some population groups in south-east Asia and Oceania
3. The red cell 3 phosphoglycerate kinase polymorphism
4. Electrophoresis of phosphoglycerate kinase
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1. Myopathic form of phosphoglycerate kinase (PGK) deficiency: A new case and pathogenic considerations;Neuromuscular Disorders;2009-03
2. Anémies hémolytiques dues à des déficits en enzymes érythrocytaires autres que la G6PD;EMC - Hématologie;2006-01
3. A novel missense mutation (1060G → C) in thephosphoglycerate kinasegene in a Japanese boy with chronic haemolytic anaemia, developmental delay and rhabdomyolysis;British Journal of Haematology;2003-09
4. Biochemical and genetic basis of red cell enzyme deficiencies;Best Practice & Research Clinical Haematology;2000-03
5. Hereditäre Membrandefekte und Enzymopathien roter Blutzellen;Monogen bedingte Erbkrankheiten 1;2000
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