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Article

Dental phenotype of the col1a2(oim) mutation: DI is present in both homozygotes and heterozygotes.

Bone - 1 Jun 2005

Lopez Franco Gloria E, Huang Alice, Pleshko Camacho Nancy, Blank Robert D

Abstract excerpt

Dentinogenesis imperfecta (DI) is a common but variable feature of osteogenesis imperfecta (OI). The Col1a2(oim) mutation (oim) is a well-studied mouse model of chain deficiency OI. Heterozygous oim/+ mice have subtle skeletal fragility, while homozygous oim/oim mice have marked skeletal fragility. To further define the consequences of oim mutation, we examined teeth by light and scanning electron microscopy...

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Identifiers

PMID: 15878701
DOI: 10.1016/j.bone.2005.03.004

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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