TY  - CHAP
M1  - Book, Section
TI  - Pyruvate Kinase Deficiency (PKD)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - It  is  a  rare,  but  most  common  hereditary  glycolytic  enzyme  defect  that  results  in  nonspherocytic  hemolytic  anemia.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/17
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164083022
ER  -