Novel MSX1 variants identified in families with nonsyndromic oligodontia

Abstract 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 familie...

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Main Authors: Jinglei Zheng (Author), Miao Yu (Author), Haochen Liu (Author), Tao Cai (Author), Hailan Feng (Author), Yang Liu (Author), Dong Han (Author)
Format: Book
Published: Nature Publishing Group, 2021-01-01T00:00:00Z.
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3rd Floor Main Library

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