A novel DSPPmutation is associated with type II dentinogenesis Imperfecta in a chinese family
Open Access
- 8 August 2007
- journal article
- Published by Springer Nature in BMC Medical Genetics
- Vol. 8 (1), 52
- https://doi.org/10.1186/1471-2350-8-52
Abstract
Hereditary defects of tooth dentin are classified into two main groups: dentin dysplasia (DD) (types I and II) and dentinogenesis imperfecta (DGI) (types I, II, and III). Type II DGI is one of the most common tooth defects with an autosomal dominant mode of inheritance. One disease-causing gene, the dentin sialophosphoprotein (DSPP) gene, has been reported for type II DGI.Keywords
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