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hexa

betahexosaminidase

taysachs

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 genetic gm2 gangliosidosis hexosaminidase deficiency lipid storage lysosomal medical metabolic neurology ocular ophthalmology opthalmology pathology rare science sphingolipidosis tsd 3d illustration molecule human alpha polypeptide chemical structure molecular biochemistry chemistry enzyme plain background atoms white space filled

Molecule Of Beta-hexosaminidase A Royalty-Free Illustration


Molecule of beta-hexosaminidase A Cartoon Illustration
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Molecule of beta-hexosaminidase A #230987631
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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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