Investigation of the genetic and clinical features of laterality disorders in prenatal diagnosis: discovery of a novel compound heterozygous mutation in the DNAH11 gene.
Simin ZhangJingjing WangLijuan SunJijing HanXiaowei XiongDan XiaoQing-Qing WuPublished in: Archives of gynecology and obstetrics (2024)
This study identified the types of CHD with a high incidence in patients with laterality disorders. It is clear that WES is an effective tool for diagnosing laterality disorders and can play an important role in future research.