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ganglioside
gm2
molecule
gangliosidosis
hexa
betahexosaminidase
taysachs
disease autosomal recessive disorder genetic hexosaminidase deficiency lipid storage lysosomal medical metabolic neurology ocular ophthalmology pathology science sphingolipidosis tsd 3d illustration human alpha polypeptide chemical structure molecular enzyme brain congenital demyelination diagram gene mutation infancy infant inherited lysosome neuron black backgroundMolecule Of Ganglioside GM2 Royalty-Free Illustration
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Molecule of Ganglioside GM2 #230989257
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