Novel MSX1 variants identified in families with nonsyndromic oligodontia

The goal of this study was to identify MSX1 gene variants in multiple Chinese families with nonsyndromic oligodontia and analyse the functional influence of these variants. Whole-exome sequencing (WES) and Sanger sequencing were performed to identify the causal gene variants in five families with no...

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Detalles Bibliográficos
Autores principales: Zheng, Jinglei, Yu, Miao, Liu, Haochen, Cai, Tao, Feng, Hailan, Liu, Yang, Han, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794556/
https://www.ncbi.nlm.nih.gov/pubmed/33419968
http://dx.doi.org/10.1038/s41368-020-00106-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794556/
https://www.ncbi.nlm.nih.gov/pubmed/33419968
http://dx.doi.org/10.1038/s41368-020-00106-0

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