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Changes of collagen in osteogenesis imperfecta

✍ Scribed by Oxlund, H.; Pedersen, U.; Danielsen, C.C.; Oxlund, I.; Elbrønd, O.


Book ID
122933787
Publisher
Elsevier Science
Year
1985
Tongue
English
Weight
285 KB
Volume
6
Category
Article
ISSN
8756-3282

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Osteogenesis Imperfecta (OI) is a heterogeneous, inherited bone disorder usually resulting from a defect in collagen synthesis or function. The Sillence classification recognises four OI subtypes of which type III is the severe, progressively deforming form. Here, we report distinctive ultrastructur