Review paper
Osteogenesis imperfecta: Clinical diagnosis, nomenclature and severity assessment
Volume: 164, Issue: 6, Pages: 1470 - 1481
Published: Apr 8, 2014
Abstract
Recently, the genetic heterogeneity in osteogenesis imperfecta (OI), proposed in 1979 by Sillence et al., has been confirmed with molecular genetic studies. At present, 17 genetic causes of OI and closely related disorders have been identified and it is expected that more will follow. Unlike most reviews that have been published in the last decade on the genetic causes and biochemical processes leading to OI, this review focuses on the clinical...
Paper Details
Title
Osteogenesis imperfecta: Clinical diagnosis, nomenclature and severity assessment
Published Date
Apr 8, 2014
Volume
164
Issue
6
Pages
1470 - 1481
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