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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Aineistotyyppi: | Artikkeli |
Kieli: | englanti |
Julkaistu: |
Philipps-Universität Marburg
2022
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Internet
PDF-kokotekstiHyllypaikka: |
urn:nbn:de:hebis:04-es2024-07697 |
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Julkaisupäivä: |
2024-01-22 |
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Erstveröffentlichung: Gehlen J, Giel AS, Köllges R, Haas SL, Zhang R, et. al. First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B. HGG Adv. 2022 Jan 25;3(2):100093. https://doi.org/10.1016/j.xhgg.2022.100093 |
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44 (2024) |
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https://creativecommons.org/licenses/by-nc-nd/4.0/ |
Linkki aineistoon: |
https://archiv.ub.uni-marburg.de/es/2024/0769 https://doi.org/10.1016/j.xhgg.2022.100093 |