The metabolism of glucocerebrosides - From 1965 to the present.
Gaucher disease is caused by the defective catabolism of the simple glycosphingolipid, glucosylceramide (GlcCer), due to mutations in the GBA1 gene which encodes for acidβ-glucosidase (GCase), the lysosomal enzyme that degrades GlcCer. Today, Gaucher disease patients are routinely treated with recom...
| Main Authors: | , |
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| Formato: | Journal article |
| Idioma: | English |
| Publicado: |
Elsevier
2016
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