TY - CHAP M1 - Book, Section TI - Phosphoglycerate Kinase Deficiency A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A rare congenital enzymatic defect in glycolysis process. It is characterized by various combinations of nonspherocytic hemolytic anemia, neurological dysfunctions, and myopathies. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164081700 ER -