A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a chinese family

BACKGROUND: 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-causi...

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Detalles Bibliográficos
Autores principales: Zhang, Xianqin, Chen, Lanying, Liu, Jingyu, Zhao, Zhen, Qu, Erjun, Wang, Xiaotao, Chang, Wei, Xu, Chengqi, Wang, Qing K, Liu, Mugen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995191/
https://www.ncbi.nlm.nih.gov/pubmed/17686168
http://dx.doi.org/10.1186/1471-2350-8-52

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995191/
https://www.ncbi.nlm.nih.gov/pubmed/17686168
http://dx.doi.org/10.1186/1471-2350-8-52

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