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Osteoblasts mineralization and collagen matrix are conserved upon specific Col1a2 silencing
Classical osteogenesis imperfecta (OI) is an inherited rare brittle bone disease caused by dominant mutations in the COL1A1 or COL1A2 genes, encoding for the α chains of collagen type I. The definitive cure for the disease will require a gene therapy approach, aimed to correct or suppress the mutant...
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| Autors principals: | , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2020-05-01
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| Col·lecció: | Matrix Biology Plus |
| Matèries: | |
| Accés en línia: | http://www.sciencedirect.com/science/article/pii/S2590028520300090 |
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