Novel molecular mechanisms leading to osteogenesis imperfecta
Osteogenesis imperfecta (OI) is an inherited disorder characterized by increased bone fragility, with severity ranging from very mild to lethal. Mutation in COL1A1 and COL1A2, which code for type I collagen, are identified in the majority (~85%) of patients. Research to identify the cause of OI in i...
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University of Sheffield
2018
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| Online Access: | https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.758358 |