A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect.

Prenatal diagnosis(2023)

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Abstract
ZIC3 encodes a highly conserved zinc-finger protein that is highly correlated with CHDs. The present study of a Han Chinese family with CHDs expands the mutation spectrum of ZIC3 and provides further evidence that ZIC3 plays important roles in CHDs.
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