Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in <i>COL1A2</i>

Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in <i>COL1A2</i>

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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Bibliographic Details
Main Authors: Yejin Lee, Youn Jung Kim, Hong-Keun Hyun, Jae-Cheoun Lee, Zang Hee Lee, Jung-Wook Kim
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Journal of Personalized Medicine
Subjects:
hereditary
mutational hotspot
dentinogenesis imperfecta
isolated dentin defect
tooth
discoloration
Online Access:https://www.mdpi.com/2075-4426/11/6/526

Internet

https://www.mdpi.com/2075-4426/11/6/526

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