RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164082868 T1 Purine Nucleoside Phosphorylase 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=1164082868 RD 2024/10/16 AB Inherited disease of the purine catabolism. Characterized by severe immunodeficiency, neurological dysfunction, and autoimmunity. Part of the ☞Severe Combined Immune deficiency Syndrome (SCIDS).