tay sachs disease illustration |
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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 pathology rare science sphingolipidosis tsd illustration molecule human alpha polypeptide chemical structure molecular enzyme background brain congenital demyelination diagram gene mutation ganglioside infancy infant inherited lysosome neuron dna |
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| Tay-Sachs disease, 3D illustration. A genetic disorder that progressively destroys brain neurons, is caused by a genetic mutation in the HEXA gene leading to deficiency of hexosaminidase A enzyme |
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