Osteogenesis Imperfecta Type VI: A Form of Brittle Bone Disease with a Mineralization Defect
Abstract
Osteogenesis imperfecta (OI) is a heritable disease of bone in which the hallmark is bone fragility. Usually, the disorder is divided into four groups on clinical grounds. We previously described a group of patients initially classified with OI type IV who had a discrete phenotype including hyperplastic callus formation without evidence of mutations in type I collagen. We called that disease entity OI type V. In this study, we describe another...
Paper Details
Title
Osteogenesis Imperfecta Type VI: A Form of Brittle Bone Disease with a Mineralization Defect
Published Date
Jan 1, 2002
Volume
17
Issue
1
Pages
30 - 38
Citation AnalysisPro
You’ll need to upgrade your plan to Pro
Looking to understand the true influence of a researcher’s work across journals & affiliations?
- Scinapse’s Top 10 Citation Journals & Affiliations graph reveals the quality and authenticity of citations received by a paper.
- Discover whether citations have been inflated due to self-citations, or if citations include institutional bias.
Notes
History