Severe Osteogenesis Imperfecta in Cyclophilin B–Deficient Mice

Osteogenesis Imperfecta (OI) is a human syndrome characterized by exquisitely fragile bones due to osteoporosis. The majority of autosomal dominant OI cases result from point or splice site mutations in the type I collagen genes, which are thought to lead to aberrant osteoid within developing bones....

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Detalles Bibliográficos
Autores principales: Choi, Jae Won, Sutor, Shari L., Lindquist, Lonn, Evans, Glenda L., Madden, Benjamin J., Bergen, H. Robert, Hefferan, Theresa E., Yaszemski, Michael J., Bram, Richard J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777385/
https://www.ncbi.nlm.nih.gov/pubmed/19997487
http://dx.doi.org/10.1371/journal.pgen.1000750

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777385/
https://www.ncbi.nlm.nih.gov/pubmed/19997487
http://dx.doi.org/10.1371/journal.pgen.1000750

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