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Alteration of proteoglycan sulfation affects bone growth and remodeling
Diastrophic dysplasia (DTD) is a chondrodysplasia caused by mutations in the SLC26A2 gene, leading to reduced intracellular sulfate pool in chondrocytes, osteoblasts and fibroblasts. Hence, proteoglycans are undersulfated in the cartilage and bone of DTD patients. To characterize the bone phenotype...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier Science
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3607217/ https://ncbi.nlm.nih.gov/pubmed/23369989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2013.01.036 |
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