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Correction: The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT.
Coughlin, Curtis R; Swanson, Michael A; Kronquist, Kathryn; Acquaviva, Cécile; Hutchin, Tim; Rodríguez-Pombo, Pilar; Väisänen, Marja-Leena; Spector, Elaine; Creadon-Swindell, Geralyn; Brás-Goldberg, Ana M; Rahikkala, Elisa; Moilanen, Jukka S; Mahieu, Vincent; Matthijs, Gert; Bravo-Alonso, Irene; Pérez-Cerdá, Celia; Ugarte, Magdalena; Vianey-Saban, Christine; Scharer, Gunter H; Van Hove, Johan L K.
Afiliação
  • Coughlin CR; Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
  • Swanson MA; Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
  • Kronquist K; Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
  • Acquaviva C; Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Children's Hospital Colorado, Aurora, Colorado, USA.
  • Hutchin T; Service Maladies Héréditaires du Métabolisme, Centre de Biologie Est, CHU de Lyon, Lyon, France.
  • Rodríguez-Pombo P; Newborn Screening and Biochemical Genetics, Birmingham Children's Hospital, Birmingham, UK.
  • Väisänen ML; 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.
  • Spector E; Research Group of Cancer Research and Translational Medicine, University of Oulu, Oulu, and Northern Finland Laboratory Centre Nordlab, Oulu, Finland.
  • Creadon-Swindell G; Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
  • Brás-Goldberg AM; Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Children's Hospital Colorado, Aurora, Colorado, USA.
  • Rahikkala E; Section of Genetics, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
  • Moilanen JS; Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Children's Hospital Colorado, Aurora, Colorado, USA.
  • Mahieu V; Newborn Screening and Biochemical Genetics, Birmingham Children's Hospital, Birmingham, UK.
  • Matthijs G; PEDEGO Research Unit, Medical Research Center, Department of Clinical Genetics, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Bravo-Alonso I; PEDEGO Research Unit, Medical Research Center, Department of Clinical Genetics, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Pérez-Cerdá C; Center for Human Genetics, University of Leuven, Leuven, Belgium.
  • Ugarte M; Center for Human Genetics, University of Leuven, Leuven, Belgium.
  • Vianey-Saban C; 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.
  • Scharer GH; 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.
  • Van Hove JLK; 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.
Genet Med ; 20(9): 1098, 2018 09.
Article em En | MEDLINE | ID: mdl-29300369
ABSTRACT
The original supplementary information included with this article contained several minor errors. Corrected Supplementary Information accompanies this corrigendum.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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XML
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos