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New Genes in Bone Development: What's New in Osteogenesis Imperfecta
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and deformity and growth deficiency. Most cases of OI (classical types) have autosomal dominant inheritance and are caused by mutations in the type I collagen genes. During the past several years, a number of...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Endocrine Society
2013
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3733862/ https://ncbi.nlm.nih.gov/pubmed/23771926 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2013-1505 |
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