Associated Papers
Application of CRISPR-Cas9 gene editing for congenital heart disease.
Seok H et al.
Clinical and Experimental Pediatrics, 2021
Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease.
Yoshida A et al.
Journal of Human Genetics, 2016
Duplication and deletion of CFC1 associated with heterotaxy syndrome.
Cao R et al.
Dna and Cell Biology, 2015
Genetic factors in non-syndromic congenital heart malformations.
Wessels MW et al.
Clinical Genetics, 2010
Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.
Selamet Tierney ES et al.
Cardiology in the Young, 2007
CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle.
Goldmuntz E et al.
American Journal of Human Genetics, 2002
Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects.
Bamford RN et al.
Nature Genetics, 2000
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