Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in COL1A2

Hereditary dentin defects can be categorized as a syndromic form predominantly related to osteogenesis imperfecta (OI) or isolated forms without other non-oral phenotypes. Mutations in the gene encoding dentin sialophosphoprotein (DSPP) have been identified to cause dentinogenesis imperfecta (DGI) T...

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Detalles Bibliográficos
Autores principales: Lee, Yejin, Kim, Youn Jung, Hyun, Hong-Keun, Lee, Jae-Cheoun, Lee, Zang Hee, Kim, Jung-Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229930/
https://www.ncbi.nlm.nih.gov/pubmed/34201399
http://dx.doi.org/10.3390/jpm11060526

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229930/
https://www.ncbi.nlm.nih.gov/pubmed/34201399
http://dx.doi.org/10.3390/jpm11060526

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