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

Johnson, Tyler B; Mechels, Keegan; Anderson, Ruthellen H; Cain, Jacob T; Sturdevant, David A; Braddock, Stephen; Pinz, Hailey; Wilson, Mark A; Landsverk, Megan; Roux, Kyle J; Weimer, Jill M

Johnson, Tyler B; Mechels, Keegan; Anderson, Ruthellen H; Cain, Jacob T; Sturdevant, David A; Braddock, Stephen; Pinz, Hailey; Wilson, Mark A; Landsverk, Megan; Roux, Kyle J; Weimer, Jill M.

Afiliación

Johnson TB; Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
Mechels K; Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
Anderson RH; Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
Cain JT; Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
Sturdevant DA; Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
Braddock S; Division of Medical Genetics, Department of Pediatrics, Saint Louis University School of Medicine, Saint Louis, Missouri, USA.
Pinz H; Division of Medical Genetics, Department of Pediatrics, Saint Louis University School of Medicine, Saint Louis, Missouri, USA.
Wilson MA; Department of Biochemistry and Redox Biology Center, University of Nebraska, Lincoln, Nebraska, USA.
Landsverk M; Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA.
Roux KJ; Pediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org.
Weimer JM; Department of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org.

Sci Rep ; 10(1): 6635, 2020 Apr 15.

Article en En | MEDLINE | ID: mdl-32296074

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

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