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Osteogenesis imperfecta (the brittle bone syndrome): Advances and controversies

โœ Scribed by Roger Smith; Bryan Sykes

Book ID
110554240
Publisher
Springer
Year
1985
Tongue
English
Weight
483 KB
Volume
37
Category
Article
ISSN
1432-0827

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Osteogenesis imperfecta (OI) is a genetic disorder of connective tissue characterized by bone fragility and alteration in synthesis and posttranslational modification of type I collagen. Autosomal dominant OI is caused by mutations in the genes (__COL1A1__ or __COL1A2__) encoding the chains of type