טוען...
Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency.
We have characterized a new mutant mouse that has virtually no beta-glucuronidase activity. This biochemical defect causes a murine lysosomal storage disease that has many interesting similarities to human mucopolysaccharidosis type VII (MPS VII; Sly syndrome; beta-glucuronidase deficiency). Genetic...
שמור ב:
| הוצא לאור ב: | J Clin Invest |
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| Main Authors: | , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Clinical Investigation
1989
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC303816/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2495302/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114010 |
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