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hexa
betahexosaminidase
taysachs
disease
autosomal
recessive
disorder
genetic gm2 gangliosidosis hexosaminidase deficiency lipid storage lysosomal medical metabolic neurology ocular ophthalmology pathology rare science sphingolipidosis tsd 3d illustration molecule human alpha polypeptide chemical structure molecular enzyme background brain congenital demyelination diagram gene mutation ganglioside infancy infant inherited lysosome neuron dnaTay-Sachs Disease, 3D Illustration
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Tay-Sachs disease, 3D illustration #230987925
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