Targeting TGFb In Osteogenesis Imperfecta
Description preview
PROJECT SUMMARY
Osteogenesis Imperfecta (OI) is a group of heterogeneous brittle bone disorders. Over 95% of patients
harbor dominantly inherited structural mutations in the type I procollagen genes (COL1A1 and COL1A2) or
recessively inherited mutations in the protein complexes important in type I collagen post-translational assembly
and…
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