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Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate
Authors:Tiit Nikopensius  Kaarel Krjutškov  Veronika Tammekivi  Mare Saag  Inga Prane  Linda Piekuse  Ilze Akota  Biruta Barkane  Astrida Krumina  Laima Ambrozaitytė  Aušra Matulevičienė  Zita Aušrelė Kučinskienė  Baiba Lace  Vaidutis Kučinskas  Andres Metspalu
Affiliation:1. Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia;2. Estonian Biocentre, Tartu, EstoniaT.N. and T.J. contributed equally to this work.;3. Estonian Genome Center, University of Tartu, Tartu, Estonia;4. Estonian Biocentre, Tartu, Estonia;5. Department of Stomatology, Faculty of Medicine, University of Tartu, Tartu, Estonia;6. Department of Biology and Microbiology, Riga Stradins University, Riga, Latvia;7. Latvian Biomedical Research and Study Center, Riga, Latvia;8. Scientific Laboratory of Human Molecular Genetics, Riga Stradins University, Riga, Latvia;9. Institute of Stomatology, Riga Stradins University, Riga, Latvia;10. Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Vilnius, Lithuania;11. Department of Physiology, Biochemistry and Laboratory Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania
Abstract:
Keywords:nonsyndromic cleft palate  case‐control association study  SNP  APEX  genotyping
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