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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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Detalhes bibliográficos
Publicado no:Int J Oral Sci
Main Authors: Zheng, Jinglei, Yu, Miao, Liu, Haochen, Cai, Tao, Feng, Hailan, Liu, Yang, Han, Dong
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7794556/
https://ncbi.nlm.nih.gov/pubmed/33419968
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41368-020-00106-0
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