First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B

Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) is the most common congenital malformation of the upper digestive tract. This study represents the first genome-wide association study (GWAS) to identify risk loci for EA/TEF. We used a European case-control sample comprising 764...

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Autores principales:	Gehlen, Jan, Giel, Ann-Sophie, Köllges, Ricarda, Bornholdt, Dorothea, Jung, Daphne, Hoyer, Paul D., Nordenskjöld, Agneta, Hess, Timo, Baumgarten, Martig, Seitz, Guido, Schumacher, Johannes
Otros Autores:	et. al.
Formato:	Artículo
Lenguaje:	inglés
Publicado:	Philipps-Universität Marburg 2022
Materias:	FOXF1/FOXC2/FOXL1 HNF1B CTNNA3 Medizin esophageal atresia (EA) multifactorial diseases genome-wide association study (GWAS) Medical sciences Medicine
Acceso en línea:	Texto Completo PDF
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