RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164081700 T1 Phosphoglycerate Kinase Deficiency T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164081700 RD 2024/04/16 AB A rare congenital enzymatic defect in glycolysis process. It is characterized by various combinations of nonspherocytic hemolytic anemia, neurological dysfunctions, and myopathies.