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Article

Novel MSX1 variants identified in families with nonsyndromic oligodontia

8 Jan 2021

Abstract excerpt

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 nonsyndromic oligodontia, and a series of bioinformatics databases were used for variant confirmation and functional...

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PMID: 33419968
DOI: 10.1038/s41368-020-00106-0

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