TY - CHAP M1 - Book, Section TI - Purine Nucleoside Phosphorylase Deficiency A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Inherited disease of the purine catabolism. Characterized by severe immunodeficiency, neurological dysfunction, and autoimmunity. Part of the ☞Severe Combined Immune deficiency Syndrome (SCIDS). SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/15 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164082868 ER -