Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome

ConclusionOur study has advanced the understanding of the genetic architecture of VWS and provides the basis for genetic counseling, antenatal diagnosis, and gene therapy of high risk groups.

Source: Molecular Genetics & Genomic Medicine - March 4, 2020 Category: Genetics & Stem Cells Authors: Yanqin Yu, Yatao Wan, Chuanqi Qin, Haitang Yue, Zhuan Bian, Miao He Tags: ORIGINAL ARTICLE Source Type: research