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[Osteogenesis imperfecta (OI) or 'brittle bone disease' is currently best described as a group of hereditary connective tissue disorders related to primary defects in type I procollagen, and to alterations in type I procollagen biosynthesis, both associated with osteoporosis and increased susceptibility to bone fractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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