A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family

BACKGROUND: Several studies have shown that the clinical phenotypes of dentinogenesis imperfecta type II (DGI-II) may be caused by mutations in dentin sialophosphoprotein (DSPP). However, no previous studies have documented the clinical phenotype and genetic basis of DGI-II in a Mongolian family fro...

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Detalles Bibliográficos
Autores principales: Bai, Haihua, Agula, Hasi, Wu, Qizhu, Zhou, Wenyu, Sun, Yujing, Qi, Yue, Latu, Suya, Chen, Yujie, Mutu, Jiri, Qiu, Changchun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829541/
https://www.ncbi.nlm.nih.gov/pubmed/20146806
http://dx.doi.org/10.1186/1471-2350-11-23

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829541/
https://www.ncbi.nlm.nih.gov/pubmed/20146806
http://dx.doi.org/10.1186/1471-2350-11-23

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