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

Gehlen, Jan; Giel, Ann-Sophie; Köllges, Ricarda; Bornholdt, Dorothea; Jung, Daphne; Hoyer, Paul D.; Nordenskjöld, Agneta; Hess, Timo; Baumgarten, Martig; Seitz, Guido; Schumacher, Johannes

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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主要な著者:	Gehlen, Jan, Giel, Ann-Sophie, Köllges, Ricarda, Bornholdt, Dorothea, Jung, Daphne, Hoyer, Paul D., Nordenskjöld, Agneta, Hess, Timo, Baumgarten, Martig, Seitz, Guido, Schumacher, Johannes
その他の著者:	et. al.
フォーマット:	論文
言語:	英語
出版事項:	Philipps-Universität Marburg 2022
主題:	genome-wide association study (GWAS) FOXF1/FOXC2/FOXL1 HNF1B CTNNA3 multifactorial diseases esophageal atresia (EA)
オンライン･アクセス:	PDFフルテキスト
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First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B

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