Identification of a novel EVC variant in a Han-Chinese family with Ellis-van Creveld syndrome.
Xiangjun HuangYi GuoHongbo XuZhijian YangXiong DengHao DengLamei YuanPublished in: Molecular genetics & genomic medicine (2019)
The identified novel homozygous EVC variant, c.2014C>T, p.(Q672*), was responsible for EVC in this Han-Chinese pedigree. The findings in this study extend the EVC mutation spectrum and may provide new insights into EVC causation and diagnosis with implications for genetic counseling and clinical management.