Definition for Revision history of "Tay-Sachs disease"

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  • (cur | prev) 14:08, 16 October 2013Padre (Talk | contribs). . (713 bytes) (+713). . (Created page with "Tay–Sachs disease (also known as GM2 gangliosidosis or hexosaminidase A deficiency) is a rare autosomal recessive genetic disorder. In its most common variant (known as infanti...")