molecule beta hexosaminidase
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molecule beta hexosaminidase |
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| navigate by keyword : hexa betahexosaminidase taysachs disease autosomal recessive disorder genetic gm2 gangliosidosis hexosaminidase deficiency lipid storage lysosomal medical metabolic neurology ocular ophthalmology opthalmology pathology rare science sphingolipidosis tsd illustration molecule human alpha polypeptide chemical structure molecular biochemistry chemistry enzyme plain background black bands |
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| 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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Stockphotos.ro (c) 2025. All stock photos are provided by Dreamstime and are copyrighted by their respective owners. |
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