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Bilateral giant retinal tears in Osteogenesis Imperfecta
BACKGROUND: Osteogenesis imperfecta (OI) is a rare primarily autosomal dominant condition in which the connective tissues of bones, ligaments and sclerae do not form properly. Typically, mutations in COL1A1 and COL1A2 genes lead to the defective formation or quantity of type I collagen, the principl...
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| Publicado no: | BMC Med Genet |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5766974/ https://ncbi.nlm.nih.gov/pubmed/29329516 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0521-0 |
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