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Osteogenesis imperfecta type 11
- ... Fragilitas ossium OI Vrolik disease Genetic Testing Registry: Osteogenesis imperfecta type 11 Genetic Testing Registry: Osteogenesis imperfecta type 13 Genetic ...
- ... C, Marini JC. Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix. Hum Mutat. 2012 Nov;33(11):1589-98. doi: 10.1002/humu.22139. Epub ...
- ... also responsible for dentin dysplasia type II. Dentinogenesis imperfecta type I occurs as part of osteogenesis imperfecta, which is caused by mutations in one ...