RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164079949
T1 N-Acetylglutamate Synthetase Deficiency
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=1164079949
RD 2024/04/24
AB Congenital  mitochondrial  disorder  of  the  metabolism  of  ammonium  (hyperammonemia)  leading  to  an  anomaly  in  the  urea  cycle.