Φορτώνει......
Delayed hypertrophic differentiation of epiphyseal chondrocytes contributes to failed secondary ossification in mucopolysaccharidosis VII dogs
Mucopolysaccharidosis (MPS) VII is a lysosomal storage disorder characterized by deficient β-glucuronidase activity, which leads to the accumulation of incompletely degraded glycosaminoglycans (GAGs). MPS VII patients present with severe skeletal abnormalities, which are particularly prevalent in th...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Mol Genet Metab |
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| Κύριοι συγγραφείς: | , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2015
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4641049/ https://ncbi.nlm.nih.gov/pubmed/26422116 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2015.09.008 |
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