TY  - CHAP
M1  - Book, Section
TI  - Histidinemia
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Histidinemia  is  a  rare  hereditary  metabolic  disorder  characterized  by  a  deficiency  of  the  enzyme  histidase,  which  is  necessary  for  the  metabolism  of  the  amino  acid  histidine.  The  majority  of  individuals  are  asymptomatic.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58080024
ER  -