![](https://wthumb.tpgimages.com/mid2_com_img/1339/29141/TPG33142496.jpg)
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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Details
Creative#:
TPG33142496
Source:
達志影像
Authorization Type:
RF
Release Information:
須由TPG 完整授權
Model Release:
N/A
Property Release:
N/A
Right to Privacy:
No
Same folder images:
hexabeta-HexosaminidaseAenzymetay-sachsdiseaseautosomalrecessivedisordergeneticgm2gangliosidosishexosaminidaseadeficiencylipidstoragelysosomalstoragediseasemedicalmetabolicneurologyocularophthalmologyophthalmologypathologyraresphingolipidosistsd3dillustrationmoleculehumanalphapolypeptidechemicalstructuremolecularbiochemistrychemistryenzymeblackbackgroundbandsartwork
3dAaalphaartworkautosomalbackgroundbandsbeta-Hexosaminidasebiochemistryblackchemicalchemistrydeficiencydiseasediseasedisorderenzymeenzymegangliosidosisgeneticgm2hexahexosaminidasehumanillustrationlipidlysosomalmedicalmetabolicmolecularmoleculeneurologyocularophthalmologyophthalmologypathologypolypeptiderarerecessivesphingolipidosisstoragestoragestructuretay-sachstsd