Molecule of beta-hexosaminidase A
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
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Keywords:
hexabetahexosaminidaseataysachsdiseaseautosomalrecessivedisordergeneticgm2gangliosidosishexosaminidasedeficiencylipidstoragelysosomalmedicalmetabolicneurologyocularophthalmologyopthalmologypathologyraresciencesphingolipidosistsd3dillustrationmoleculehumanalphapolypeptidechemicalstructuremolecularbiochemistrychemistryenzymeplainbackgroundatomswhitespacefilled
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Image ID: 230987631