Associated Papers
Correlations between ISL1 rs1017 polymorphism and congenital heart disease risk: A PRISMA-compliant meta-analysis.
Ding Z et al.
Medicine, 2020
A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle.
Wang Z et al.
International Heart Journal, 2019
ISL1 loss-of-function mutation contributes to congenital heart defects.
Ma L et al.
Heart and Vessels, 2019
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