RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164083022 T1 Pyruvate Kinase Deficiency (PKD) T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164083022 RD 2024/03/28 AB It is a rare, but most common hereditary glycolytic enzyme defect that results in nonspherocytic hemolytic anemia.