TY  - CHAP
M1  - Book, Section
TI  - Gangliosidosis (GM2) Type II
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Heritable  lysosomal  storage  disorder  with  ganglioside  accumulation  leading  to  severe  neurologic  impairment  with  premature  death.  Tay-Sachs  disease  (TSD)  and  its  variants  are  caused  by  absence  or  defects  of  the  alpha  subunit  of  hexosaminidase  A.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58077532
ER  -