Your browser doesn't support javascript.
loading
Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies.
Morava, Eva; Tiemes, Vera; Thiel, Christian; Seta, Nathalie; de Lonlay, Pascale; de Klerk, Hans; Mulder, Margot; Rubio-Gozalbo, Estela; Visser, Gepke; van Hasselt, Peter; Horovitz, Dafne D G; de Souza, Carolina Fischinger Moura; Schwartz, Ida V D; Green, Andrew; Al-Owain, Mohammed; Uziel, Graciella; Sigaudy, Sabine; Chabrol, Brigitte; van Spronsen, Franc-Jan; Steinert, Martin; Komini, Eleni; Wurm, Donald; Bevot, Andrea; Ayadi, Addelkarim; Huijben, Karin; Dercksen, Marli; Witters, Peter; Jaeken, Jaak; Matthijs, Gert; Lefeber, Dirk J; Wevers, Ron A.
Afiliación
  • Morava E; Center for Metabolic Diseases, Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium. eva.morava@uzleuven.be.
  • Tiemes V; Tulane University Medical School, Hayward Genetics Center, New Orleans, LA, USA. eva.morava@uzleuven.be.
  • Thiel C; Department of Pediatrics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Seta N; Translational Metabolic Laboratory, Department Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
  • de Lonlay P; Center for Child and Adolescent Medicine, Kinderheilkunde I, University of Heidelberg, Heidelberg, Germany.
  • de Klerk H; Biochimie Métabolique Hôpital Bichat-Claude Bernard, Paris, France.
  • Mulder M; Reference Center of Metabolism, Necker-Enfants Malades Hospital, APHP, Imagine Institute, University Paris-Descartes, Paris, France.
  • Rubio-Gozalbo E; Department of Pediatrics, Erasmus MC - University Medical Center Rotterdam, Emma Hospital, Rotterdam, The Netherlands.
  • Visser G; Department of Pediatrics, Free University Amsterdam, Amsterdam, The Netherlands.
  • van Hasselt P; Department of Pediatrics and Laboratory Genetic Metabolic Diseases, University of Maastricht, Maastricht, The Netherlands.
  • Horovitz DDG; Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • de Souza CFM; Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Schwartz IVD; Medical Genetics Service, Porto Alegre, RS, Brazil.
  • Green A; Medical Genetics Service, Porto Alegre, RS, Brazil.
  • Al-Owain M; Medical Genetics Service, Porto Alegre, RS, Brazil.
  • Uziel G; National Centre for Medical Genetics, Dublin, Ireland.
  • Sigaudy S; Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Chabrol B; University of Milan, Institute of Neurology, Milan, Italy.
  • van Spronsen FJ; Département de Génétique Médicale, Hôpital Timone Enfant, Marseille, France.
  • Steinert M; Neuropediatrics Unit, Childrens Hospital CHU Timone, Marseille, France.
  • Komini E; Division of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center of Groningen, University of Groningen, Groningen, The Netherlands.
  • Wurm D; Sozialpädiatrisches Zentrum, Neuropädiatrie, Klinik für Kinder- und Jugendmedizin, Dortmund, Germany.
  • Bevot A; Kinderklinik Villingen, Schwarzwald-Baar-Klinikum, Villingen, Germany.
  • Ayadi A; Department of Pediatrics, Klinikum Saarbrücken, Saarbrücken, Germany.
  • Huijben K; Department of Pediatric Neurology and Developmental Medicine, Universal Children's Hospital Tübingen, Tübingen, Germany.
  • Dercksen M; Biochimie Métabolique Hôpital Bichat-Claude Bernard, Paris, France.
  • Witters P; Translational Metabolic Laboratory, Department Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Jaeken J; Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.
  • Matthijs G; Center for Metabolic Diseases, Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
  • Lefeber DJ; Center for Metabolic Diseases, Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
  • Wevers RA; Laboratory for Molecular Diagnosis, Center for Human Genetics, University of Leuven, Leuven, Belgium.
J Inherit Metab Dis ; 39(5): 759, 2016 09.
Article en En | MEDLINE | ID: mdl-27498540
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Inherit Metab Dis Año: 2016 Tipo del documento: Article País de afiliación: Bélgica
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Inherit Metab Dis Año: 2016 Tipo del documento: Article País de afiliación: Bélgica