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  - 2024/04/16
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164082868
ER  -