Phenotype and molecular characterizations of a family with dentinogenesis imperfecta shields type II with a novel DSPP mutation

BACKGROUND: Dentinogenesis imperfecta (DGI), Shields type-II is an autosomal dominant genetic disease which severely affects the function of the patients’ teeth. The dentin sialophosphoprotein (DSPP) gene is considered to be the pathogenic gene of DGI-II. In this study, a DGI-II family with a novel...

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Detalles Bibliográficos
Autores principales: Du, Qin, Cao, Li, Liu, Yi, Pang, Chunyan, Wu, Si, Zheng, Liwei, Jiang, Wei, Na, Xiaoxue, Yu, Jing, Wang, Shasha, Zhu, Xianjun, Yang, Jiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8667123/
https://www.ncbi.nlm.nih.gov/pubmed/34988181
http://dx.doi.org/10.21037/atm-21-5369

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8667123/
https://www.ncbi.nlm.nih.gov/pubmed/34988181
http://dx.doi.org/10.21037/atm-21-5369

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