| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5891956 | Bone | 2012 | 7 Pages |
Abstract
⺠New FKBP10 mutation has been found. ⺠FKB10 mutation could cause OI with a mineralization defect. ⺠OI phenotype due to FKBP10 mutations is various but it seems to be progressive and the prognosis improves with biphosphonate treatment. ⺠Genetic heterogeneity has been confirmed in osteogenesis imperfecta.
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Authors
Giacomo Venturi, Elena Monti, Luca Dalle Carbonare, Massimiliano Corradi, Alberto Gandini, Maria Teresa Valenti, Attilio Boner, Franco Antoniazzi,