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.
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Creative#:
TPG33142495
Source:
達志影像
Authorization Type:
RF
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須由TPG 完整授權
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Same folder images:
hexabeta-HexosaminidaseAtay-sachsdiseaseautosomalrecessivedisordergeneticgm2gangliosidosishexosaminidaseadeficiencylipidstoragelysosomalstoragediseasemedicalmetabolicneurologyocularophthalmologyophthalmologypathologyraresphingolipidosistsd3dillustrationmoleculehumanalphapolypeptidechemicalstructuremolecularbiochemistrychemistryenzymeatomswhitebackgroundspacefilledartwork
3dAaalphaartworkatomsautosomalbackgroundbeta-Hexosaminidasebiochemistrychemicalchemistrydeficiencydiseasediseasedisorderenzymefilledgangliosidosisgeneticgm2hexahexosaminidasehumanillustrationlipidlysosomalmedicalmetabolicmolecularmoleculeneurologyocularophthalmologyophthalmologypathologypolypeptiderarerecessivespacesphingolipidosisstoragestoragestructuretay-sachstsdwhite
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