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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...

詳細記述

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書誌詳細
出版年:Int J Oral Sci
主要な著者: Zheng, Jinglei, Yu, Miao, Liu, Haochen, Cai, Tao, Feng, Hailan, Liu, Yang, Han, Dong
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group UK 2021
主題:
オンライン・アクセス: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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