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

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...

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Detalles Bibliográficos
Autores principales: Andersson, Kristofer, Dahllöf, Göran, Lindahl, Katarina, Kindmark, Andreas, Grigelioniene, Giedre, Åström, Eva, Malmgren, Barbro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428910/
https://www.ncbi.nlm.nih.gov/pubmed/28498836
http://dx.doi.org/10.1371/journal.pone.0176466

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428910/
https://www.ncbi.nlm.nih.gov/pubmed/28498836
http://dx.doi.org/10.1371/journal.pone.0176466

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