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Genz-682452

National Institutes of Health

Papers overview

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2019
2019
Neuronopathic glycosphingolipidoses are a sub-group of lysosomal storage disorders for which there are presently no effective… Expand
Highly Cited
2016
Highly Cited
2016
Gaucher disease (GD) is caused by a deficiency of glucocerebrosidase and the consequent lysosomal accumulation of unmetabolized… Expand
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Highly Cited
2015
Highly Cited
2015
Fabry disease, an X-linked glycosphingolipid storage disorder, is caused by the deficient activity of α-galactosidase A (α-Gal A… Expand
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