Characterization of novel MSX1 variants causally associated with non ‐syndromic oligodontia in Chinese families

ConclusionThree novelMSX1 variants were identified in Chinese Han families with NSO, expanding theMSX1 variant spectrum and presenting a genetic origin for the pathogenesis detected in patients and their families.

Source: Molecular Genetics & Genomic Medicine - December 9, 2023 Category: Genetics & Stem Cells Authors: Ya Zhao, Jiabao Ren, Lingqiang Meng, Yan Hou, Chunyan Liu, Guozhong Zhang, Wenjing Shen Tags: ORIGINAL ARTICLE Source Type: research