RNF41

Association between RNF41 gene c.-206 T > A genetic polymorphism and risk of congenital heart diseases in the Chinese Mongolian population

Y. Zhang, Jin, S. Q., Li, W. X., Gao, G. Q., Zhang, K., Huang, J. L., Zhang, Y., Jin, S. Q., Li, W. X., Gao, G. Q., Zhang, K., and Huang, J. L., Association between RNF41 gene c.-206 T > A genetic polymorphism and risk of congenital heart diseases in the Chinese Mongolian population, vol. 15, p. -, 2016.

This study aimed to explore the association between ring finger protein 41 (RNF41) c.-206 T > A variant and susceptibility to congenital heart disease (CHD) in the Chinese Mongolian population. The association between RNF41 gene c.-206 T > A polymorphism and CHD was examined in two independent case-control studies consisting of 219 CHD patients and 208 healthy controls. Genotype was determined by direct sequencing of PCR products.

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