| ganglioside | ||||||||||||||||||||||||||||||||||||||||
| navigate by keyword : 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 illustration human alpha polypeptide chemical structure molecular enzyme brain congenital demyelination diagram gene mutation infancy infant inherited lysosome neuron black background | ||||||||||||||||||||||||||||||||||||||||
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| Molecule of Ganglioside GM2, 3D illustration. It is associated with GM2 gangliosidoses such as Tay-Sachs disease that progressively destroys brain neurons due to accumulation of ganglioside in neurons | ||||||||||||||||||||||||||||||||||||||||
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