טוען...
Effective cell and gene therapy in a murine model of Gaucher disease
Gaucher disease (GD) is a lysosomal storage disorder due to an inherited deficiency in the enzyme glucosylceramidase (GCase) that causes hepatosplenomegaly, cytopenias, and bone disease as key clinical symptoms. Previous mouse models with GCase deficiency have been lethal in the perinatal period or...
שמור ב:
| Main Authors: | , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
National Academy of Sciences
2006
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1564262/ https://ncbi.nlm.nih.gov/pubmed/16954197 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0606016103 |
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