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. | |
Lizenzart: | Lizenzfrei |
Credit: | Science Photo Library / Kon, Kateryna |
Modell-Rechte: | nicht erforderlich |
Eigentums-Rechte: | nicht erforderlich |
Restrictions: | - |