hexosaminidasa A [Hexosaminidase A]

tematický
1
Termíny

Hex A
hexosaminidáza A
hexozaminidáza A

 

beta-N-Acetylhexosaminidase A
Hex A

Perzistentní odkaz   https://www.medvik.cz/link/D054818
Definice

A mammalian beta-hexosaminidase isoform that is a heteromeric protein comprized of both hexosaminidase alpha and hexosaminidase beta subunits. Deficiency of hexosaminidase A due to mutations in the gene encoding the hexosaminidase alpha subunit is a case of TAY-SACHS DISEASE. Deficiency of hexosaminidase A and HEXOSAMINIDASE B due to mutations in the gene encoding the hexosaminidase beta subunit is a case of SANDHOFF DISEASE.

Anotace
for deficiency consider: SANDHOFF DISEASE or TAY-SACHS DISEASE
DUI
D054818 MeSH Prohlížeč
CUI
M0002425
RN
EC 3.2.1.52
Předchozí užití
beta-N-Acetylhexosaminidases (1999-2007)
Historická pozn.
2008(1987); for HEXOSAMINIDASE A use BETA-N-ACETYLHEXOSAMINIDASE 1987-2007
Veřejná pozn.
2008; for HEXOSAMINIDASE A see BETA-N-ACETYLHEXOSAMINIDASE 1987-2007