Загрузка...
The effect of Tlr4 and/or C3 Deficiency and of Neonatal Gene Therapy on Skeletal Disease in Mucopolysaccharidosis VII mice
Mucopolysaccharidosis (MPS) VII is a lysosomal storage disorder caused by the deficiency of the enzyme β-glucuronidase (Gusb(-/-)) and results in glycosaminoglycan (GAG) accumulation. Skeletal abnormalities include stunted long bones and bone degeneration. GAGs have been hypothesized to activate tol...
Сохранить в:
| Опубликовано в: : | Mol Genet Metab |
|---|---|
| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2014
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4381425/ https://ncbi.nlm.nih.gov/pubmed/25559179 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2014.12.305 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|