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Article

Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.

PloS one - 1 Jan 2017

Andersson Kristofer, Dahllöf Göran, Lindahl Katarina, Kindmark Andreas, Grigelioniene Giedre, Åström Eva, Malmgren Barbro

Abstract excerpt

Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused mainly by mutations in the collagen I genes (COL1A1 and COL1A2). Dentinogenesis imperfecta (DGI) and other dental aberrations are common features of OI. We investigated the association between collagen I mutations and DGI, taurodontism, and retention of permanent second molars in a retrospective cohort of 152 unrelated...

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Source

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Identifiers

PMID: 28498836
DOI: 10.1371/journal.pone.0176466
PMCID: PMC5428910

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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