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Failures of Endochondral Ossification in the Mucopolysaccharidoses
PURPOSE OF REVIEW: The mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders characterized by abnormal accumulation of glycosaminoglycans (GAGs) in cells and tissues. MPS patients frequently exhibit failures of endochondral ossification during postnatal growth leading to s...
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| Опубликовано в: : | Curr Osteoporos Rep |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2020
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7736118/ https://ncbi.nlm.nih.gov/pubmed/33064251 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11914-020-00626-y |
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