HAL (France)
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From collagen denaturation caused by a COL1A2 variant to mineral disorganization and tubular occlusion in primary dentin with dentinogenesis imperfecta
Dentinogenesis Imperfecta (DI) is a rare genetic disorder that disrupts the structure and mechanical integrity of dentin, often through alterations to the collagen matrix. In cases associated with Osteogenesis Imperfecta, DI arises from COL1A1 or COL1A2 variants (DI type I). The multiscale mechanism
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