Molecule of beta-hexosaminidase A enzyme, or HEXA, illustration. Mutations in the gene encoding HEXA decrease the hydrolysis of GM2 gangliosides, which is the main cause of Tay-Sachs disease. | |
Licence : | Libre de droits |
Crédit: | Science Photo Library / Kon, Kateryna |
Model Release : | Non requis |
Property Release : | Non requis |
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