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Management of Osteogenesis Imperfecta

Osteogenesis imperfecta (OI) is the term used to describe a group of rare inherited skeletal disorders characterized by a greatly increased risk of fragility fractures (1). Mutations in several genes can cause OI but the condition is most commonly caused by mutations of COLIA1 or COL1A2 resulting in...

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Bibliografski detalji
Izdano u:Front Endocrinol (Lausanne)
Glavni autori: Ralston, Stuart H., Gaston, Mark S.
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2020
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7026366/
https://ncbi.nlm.nih.gov/pubmed/32117044
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2019.00924
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