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Bone Collagen: New Clues to its Mineralization Mechanism From Recessive Osteogenesis Imperfecta
Until 2006 the only mutations known to cause osteogenesis imperfecta (OI) were in the two genes coding for type I collagen chains. These dominant mutations affecting the expression or primary sequence of collagen α1(I) and α2(I) chains account for over 90% of OI cases. Since then a growing list of m...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3758449/ https://ncbi.nlm.nih.gov/pubmed/23508630 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00223-013-9723-9 |
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