Fkbp10 Deletion in Osteoblasts leads to Qualitative Defects in Bone

Osteogenesis Imperfecta (OI), also known as brittle bone disease, displays a spectrum of clinical severity from mild (OI type I) to severe early lethality (OI type II), with clinical features including low bone mass, fractures and deformities. Mutations in the FK506 Binding Protein 10 (FKBP10), gene...

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Argitaratua izan da:J Bone Miner Res
Egile Nagusiak: Lietman, Caressa D., Lim, Joohyun, Grafe, Ingo, Chen, Yuqing, Ding, Hao, Bi, Xiaohong, Ambrose, Catherine G., Fratzl-Zelman, Nadja, Roschger, Paul, Klaushofer, Klaus, Wagermaier, Wolfgang, Schmidt, Ingo, Fratzl, Peter, Rai, Jyoti, Weis, MaryAnn, Eyre, David, Keene, Douglas R., Krakow, Deborah, Lee, Brendan H.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2017
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Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5466482/
https://ncbi.nlm.nih.gov/pubmed/28206698
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.3108
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