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gm2-gangliosidosis
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GM2A
Characterization of full-length cDNAs and the gene coding for the human GM2 activator protein
HEXA
Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes
A glycine250--> aspartate substitution in the alpha-subunit of hexosaminidase A causes juvenile-onset Tay-Sachs disease in a Lebanese-Canadian family
Novel Tay-Sachs disease mutations from China
Cancer Gene Census
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Definition
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Pathways
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Glycosphingolipid biosynthesis
globo series
one gene
Clinical Trials
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