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PTH treatment is effective in the Aga2/+ mouse model of moderate to severe osteogenesis imperfecta

Kot, Alexander et al.
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32 biomedical and clinical sciences (for-2020), 3202 clinical sciences (for-2020), orphan drug (rcdc), pediatric research initiative (rcdc), osteogenesis imperfecta (rcdc), rare diseases (rcdc), genetics (rcdc), congenital structural anomalies (rcdc)
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