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G(M2) Ganglioside

Tay-Sachs Disease Ganglioside | Ganglioside GM2 | GM2, Ganglioside | Ganglioside, Tay-Sachs Disease | Tay Sachs Disease Ganglioside

A glycosphingolipid that accumulates due to a deficiency of hexosaminidase A or B (BETA-N-ACETYLHEXOSAMINIDASE), or GM2 activator protein, resulting in GANGLIOSIDOSES, heredity metabolic disorders that include TAY-SACHS DISEASE and SANDHOFF DISEASE.
 
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