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Osteogenesis imperfecta—pathophysiology and therapeutic options
Osteogenesis imperfecta (OI) is a rare congenital disease with a wide spectrum of severity characterized by skeletal deformity and increased bone fragility as well as additional, variable extraskeletal symptoms. Here, we present an overview of the genetic heterogeneity and pathophysiological backgro...
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| Gepubliceerd in: | Mol Cell Pediatr |
|---|---|
| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Springer Berlin Heidelberg
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7427672/ https://ncbi.nlm.nih.gov/pubmed/32797291 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40348-020-00101-9 |
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