Correction: The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT

Curtis R Coughlin¹, Michael A Swanson¹, Kathryn Kronquist^{1

2}, Cécile Acquaviva³, Tim Hutchin⁴, Pilar Rodríguez-Pombo⁵, Marja-Leena Väisänen⁶, Elaine Spector^{1

2}, Geralyn Creadon-Swindell^{1

2}, Ana M Brás-Goldberg⁴, Elisa Rahikkala⁷, Jukka S Moilanen⁷, Vincent Mahieu⁸, Gert Matthijs⁸, Irene Bravo-Alonso⁵, Celia Pérez-Cerdá⁵, Magdalena Ugarte⁵, Christine Vianey-Saban³, Gunter H Scharer^{1

9}, Johan L K Van Hove¹⁰

Affiliations

¹ Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
² Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Children's Hospital Colorado, Aurora, Colorado, USA.
³ Service Maladies Héréditaires du Métabolisme, Centre de Biologie Est, CHU de Lyon, Lyon, France.
⁴ Newborn Screening and Biochemical Genetics, Birmingham Children's Hospital, Birmingham, UK.
⁵ Centro de Diagnóstico de Enfermedades Moleculares (CEDEM), CBM-SO, (UAM-CISC), Centro de Investigación en Red de Enfermedades Raras (CIBERER), IDIPAZ, Universidad Autónoma Madrid, Madrid, Spain.
⁶ Research Group of Cancer Research and Translational Medicine, University of Oulu, Oulu, and Northern Finland Laboratory Centre Nordlab, Oulu, Finland.
⁷ PEDEGO Research Unit, Medical Research Center, Department of Clinical Genetics, Oulu University Hospital and University of Oulu, Oulu, Finland.
⁸ Center for Human Genetics, University of Leuven, Leuven, Belgium.
⁹ Section of Medical Genetics and Genomics, Children's Hospitals and Clinics of Minnesota, Minneapolis, Minnesota, USA.
¹⁰ Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA. Johan.Vanhove@childrenscolorado.org.

PMID: 29300369
DOI: 10.1038/gim.2017.232

Free article

Published Erratum

Correction: The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT

Curtis R Coughlin et al. Genet Med. 2018 Sep.

Free article

. 2018 Sep;20(9):1098.

doi: 10.1038/gim.2017.232.

Authors

Affiliations

¹ Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
² Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Children's Hospital Colorado, Aurora, Colorado, USA.
³ Service Maladies Héréditaires du Métabolisme, Centre de Biologie Est, CHU de Lyon, Lyon, France.
⁴ Newborn Screening and Biochemical Genetics, Birmingham Children's Hospital, Birmingham, UK.
⁵ Centro de Diagnóstico de Enfermedades Moleculares (CEDEM), CBM-SO, (UAM-CISC), Centro de Investigación en Red de Enfermedades Raras (CIBERER), IDIPAZ, Universidad Autónoma Madrid, Madrid, Spain.
⁶ Research Group of Cancer Research and Translational Medicine, University of Oulu, Oulu, and Northern Finland Laboratory Centre Nordlab, Oulu, Finland.
⁷ PEDEGO Research Unit, Medical Research Center, Department of Clinical Genetics, Oulu University Hospital and University of Oulu, Oulu, Finland.
⁸ Center for Human Genetics, University of Leuven, Leuven, Belgium.
⁹ Section of Medical Genetics and Genomics, Children's Hospitals and Clinics of Minnesota, Minneapolis, Minnesota, USA.
¹⁰ Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA. Johan.Vanhove@childrenscolorado.org.

PMID: 29300369
DOI: 10.1038/gim.2017.232

Abstract

The original supplementary information included with this article contained several minor errors. Corrected Supplementary Information accompanies this corrigendum.

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Erratum for

The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT.
Coughlin CR 2nd, Swanson MA, Kronquist K, Acquaviva C, Hutchin T, Rodríguez-Pombo P, Väisänen ML, Spector E, Creadon-Swindell G, Brás-Goldberg AM, Rahikkala E, Moilanen JS, Mahieu V, Matthijs G, Bravo-Alonso I, Pérez-Cerdá C, Ugarte M, Vianey-Saban C, Scharer GH, Van Hove JL. Coughlin CR 2nd, et al. Genet Med. 2017 Jan;19(1):104-111. doi: 10.1038/gim.2016.74. Epub 2016 Jun 30. Genet Med. 2017. PMID: 27362913

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Correction: The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT

Affiliations

Correction: The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT

Authors

Affiliations

Abstract

Erratum for

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LinkOut - more resources

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