polypeptide N-acetylgalactosaminyltransferase 11 [Danio rerio]

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LOF variants identifying candidate genes of laterality defects patients with congenital heart disease. [PLoS Genet. 2022]
LOF variants identifying candidate genes of laterality defects patients with congenital heart disease.
Liu S, Wei W, Wang P, Liu C, Jiang X, Li T, Li F, Wu Y, Chen S, Sun K, et al. PLoS Genet. 2022 Dec; 18(12):e1010530. Epub 2022 Dec 2.
Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects. [Genome Med. 2018]
Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects.
Liu C, Cao R, Xu Y, Li T, Li F, Chen S, Xu R, Sun K. Genome Med. 2018 May 30; 10(1):40. Epub 2018 May 30.
Genome-wide association study of kidney function decline in individuals of European descent. [Kidney Int. 2015]
Genome-wide association study of kidney function decline in individuals of European descent.
Gorski M, Tin A, Garnaas M, McMahon GM, Chu AY, Tayo BO, Pattaro C, Teumer A, Chasman DI, Chalmers J, et al. Kidney Int. 2015 May; 87(5):1017-29. Epub 2014 Dec 10.

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