Recent developments in osteogenesis imperfecta

Osteogenesis imperfecta (OI) is an uncommon genetic bone disease associated with brittle bones and fractures in children and adults. Although OI is most commonly associated with mutations of the genes for type I collagen, many other genes (some associated with type I collagen processing) have now be...

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Detalles Bibliográficos
Autores principales: Shaker, Joseph L., Albert, Carolyne, Fritz, Jessica, Harris, Gerald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566283/
https://www.ncbi.nlm.nih.gov/pubmed/26401268
http://dx.doi.org/10.12688/f1000research.6398.1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566283/
https://www.ncbi.nlm.nih.gov/pubmed/26401268
http://dx.doi.org/10.12688/f1000research.6398.1

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