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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Marini, Joan C., Blissett, Angela R.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Endocrine Society 2013
Pynciau:
Mynediad Ar-lein: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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