Hexosaminidase A Pathway
created 17 Jun, 10:23 pm · ⏱ built in 1m 16s · 👁 2 views
Shows Tay-Sachs disease: a HEXA mutation causes hexosaminidase A deficiency, so GM2 ganglioside builds up in neurons and leads to neurodegeneration and a cherry-red macula. Tap the pathway cards to expand each step, switch between normal and disease in the lysosome tab, and answer the multiple-choice question.
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Second Year Medical School Student
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