Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen

Overview of attention for article published in Frontiers in Genetics, January 2022

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New Research: Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen: Osteogenesis imperfecta (OI) is a rare inherited connective tissue dysplasia characterized with skeletal… https://t.co/v

28 Jan 2022

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