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Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1.

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第一作者： Tyler B,Johnson

第一单位： Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.

作者： Tyler B,Johnson ^[1] ; Keegan,Mechels ^[1] ; Ruthellen H,Anderson ^[1] ; Jacob T,Cain ^[1] ; David A,Sturdevant ^[1] ; Stephen,Braddock ^[2] ; Hailey,Pinz ^[2] ; Mark A,Wilson ^[3] ; Megan,Landsverk ^[4] ; Kyle J,Roux ^[5] ; Jill M,Weimer ^[6]

作者单位： Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. ^[1] Division of Medical Genetics, Department of Pediatrics, Saint Louis University School of Medicine, Saint Louis, Missouri, USA. ^[2] Department of Biochemistry and Redox Biology Center, University of Nebraska, Lincoln, Nebraska, USA. ^[3] Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA. ^[4] Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org.;Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org. ^[5] Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. jill.weimer@sanfordhealth.org.;Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA. jill.weimer@sanfordhealth.org. ^[6]