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- [17] Similar COL1A1 expression in fibroblasts from some patients with clinical otosclerosis and those with type I osteogenesis imperfecta ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 2002, 111 (02): : 184 - 189
- [18] Case Report: A novel de novo variant of COL1A1 in fetal genetic osteogenesis imperfecta FRONTIERS IN ENDOCRINOLOGY, 2023, 14
- [19] Nuclear retention of COL1A1 messenger RNA identifies null alleles causing mild osteogenesis imperfecta JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (04): : 1035 - 1040