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Stock image Molecule of beta-hexosaminidase A enzyme, or HEXA, 3D illustration. Mutations in the gene encoding HEXA decrease the hydrolysis of GM2 gangliosides, which is the main cause of Tay-Sachs disease
Published:
Oct.05, 2021 13:09:30
Author:
katerynakon
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Beta Hexosaminidase A
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