Author Correction: Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1

Affiliations

¹ Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
² Division of Medical Genetics, Department of Pediatrics, Saint Louis University School of Medicine, Saint Louis, Missouri, USA.
³ Department of Biochemistry and Redox Biology Center, University of Nebraska, Lincoln, Nebraska, USA.
⁴ Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA.
⁵ Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org.
⁶ Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org.
⁷ Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. jill.weimer@sanfordhealth.org.
⁸ Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA. jill.weimer@sanfordhealth.org.

Published Erratum

Tyler B Johnson et al. Sci Rep. 2020.

. 2020 Apr 15;10(1):6635.

doi: 10.1038/s41598-020-62950-8.

¹ Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
² Division of Medical Genetics, Department of Pediatrics, Saint Louis University School of Medicine, Saint Louis, Missouri, USA.
³ Department of Biochemistry and Redox Biology Center, University of Nebraska, Lincoln, Nebraska, USA.
⁴ Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA.
⁵ Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org.
⁶ Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org.
⁷ Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. jill.weimer@sanfordhealth.org.
⁸ Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA. jill.weimer@sanfordhealth.org.

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1.
Johnson TB, Mechels K, Anderson RH, Cain JT, Sturdevant DA, Braddock S, Pinz H, Wilson MA, Landsverk M, Roux KJ, Weimer JM. Johnson TB, et al. Sci Rep. 2018 Nov 1;8(1):16161. doi: 10.1038/s41598-018-34437-0. Sci Rep. 2018. PMID: 30385778 Free PMC article.