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g(m2) activator protein?
An essential cofactor for the degradation of G(M2)GANGLIOSIDE by lysosomal BETA-N-ACETYLHEXOSAMINIDASES. Genetic mutations resulting in loss of G(M2) activator protein are one of the causes of TAY-SACHS DISEASE, AB VARIANT.

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fyock, fyodor, fyodor's, g, g's, g., g.'s, g.s, ga, gaal


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