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.

doi:10.1007/s10545-016-9967-4

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

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Published: 08 August 2016

Volume 39, page 759, (2016)
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Journal of Inherited Metabolic Disease

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

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Eva Morava^1,2,
Vera Tiemes^3,4,
Christian Thiel⁵,
Nathalie Seta⁶,
Pascale de Lonlay⁷,
Hans de Klerk⁸,
Margot Mulder⁹,
Estela Rubio-Gozalbo¹⁰,
Gepke Visser¹¹,
Peter van Hasselt¹¹,
Dafne D. G. Horovitz¹²,
Carolina Fischinger Moura de Souza¹²,
Ida V. D. Schwartz¹²,
Andrew Green¹³,
Mohammed Al-Owain¹⁴,
Graciella Uziel¹⁵,
Sabine Sigaudy¹⁶,
Brigitte Chabrol¹⁷,
Franc-Jan van Spronsen¹⁸,
Martin Steinert¹⁹,
Eleni Komini²⁰,
Donald Wurm²¹,
Andrea Bevot²²,
Addelkarim Ayadi⁶,
Karin Huijben⁴,
Marli Dercksen²³,
Peter Witters¹,
Jaak Jaeken¹,
Gert Matthijs²⁴,
Dirk J. Lefeber^4,25 &
…
Ron A. Wevers⁴

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The Original Article was published on 10 June 2016

Erratum to: J Inherit Metab Dis

DOI 10.1007/s10545-016-9945-x

The name of the author Christian Thiel was rendered wrongly in the original publication but has since been corrected.

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Authors and Affiliations

Center for Metabolic Diseases, Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium
Eva Morava, Peter Witters & Jaak Jaeken
Tulane University Medical School, Hayward Genetics Center, New Orleans, LA, USA
Eva Morava
Department of Pediatrics, Radboud University Medical Center, Nijmegen, The Netherlands
Vera Tiemes
Translational Metabolic Laboratory, Department Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands
Vera Tiemes, Karin Huijben, Dirk J. Lefeber & Ron A. Wevers
Center for Child and Adolescent Medicine, Kinderheilkunde I, University of Heidelberg, Heidelberg, Germany
Christian Thiel
Biochimie Métabolique Hôpital Bichat-Claude Bernard, Paris, France
Nathalie Seta & Addelkarim Ayadi
Reference Center of Metabolism, Necker-Enfants Malades Hospital, APHP, Imagine Institute, University Paris-Descartes, Paris, France
Pascale de Lonlay
Department of Pediatrics, Erasmus MC – University Medical Center Rotterdam, Emma Hospital, Rotterdam, The Netherlands
Hans de Klerk
Department of Pediatrics, Free University Amsterdam, Amsterdam, The Netherlands
Margot Mulder
Department of Pediatrics and Laboratory Genetic Metabolic Diseases, University of Maastricht, Maastricht, The Netherlands
Estela Rubio-Gozalbo
Wilhelmina Children’s Hospital, University Medical Center Utrecht, Utrecht, The Netherlands
Gepke Visser & Peter van Hasselt
Medical Genetics Service, Porto Alegre, RS, Brazil
Dafne D. G. Horovitz, Carolina Fischinger Moura de Souza & Ida V. D. Schwartz
National Centre for Medical Genetics, Dublin, Ireland
Andrew Green
Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
Mohammed Al-Owain
University of Milan, Institute of Neurology, Milan, Italy
Graciella Uziel
Département de Génétique Médicale, Hôpital Timone Enfant, Marseille, France
Sabine Sigaudy
Neuropediatrics Unit, Childrens Hospital CHU Timone, Marseille, France
Brigitte Chabrol
Division of Metabolic Diseases, Beatrix Children’s Hospital, University Medical Center of Groningen, University of Groningen, Groningen, The Netherlands
Franc-Jan van Spronsen
Sozialpädiatrisches Zentrum, Neuropädiatrie, Klinik für Kinder- und Jugendmedizin, Dortmund, Germany
Martin Steinert
Kinderklinik Villingen, Schwarzwald-Baar-Klinikum, Villingen, Germany
Eleni Komini
Department of Pediatrics, Klinikum Saarbrücken, Saarbrücken, Germany
Donald Wurm
Department of Pediatric Neurology and Developmental Medicine, Universal Children’s Hospital Tübingen, Tübingen, Germany
Andrea Bevot
Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa
Marli Dercksen
Laboratory for Molecular Diagnosis, Center for Human Genetics, University of Leuven, Leuven, Belgium
Gert Matthijs
Department of Neurology, Radboud University Medical Center, Nijmegen, The Netherlands
Dirk J. Lefeber

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Eva Morava
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Vera Tiemes
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Christian Thiel
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Nathalie Seta
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Pascale de Lonlay
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Hans de Klerk
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Margot Mulder
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Estela Rubio-Gozalbo
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Gepke Visser
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Peter van Hasselt
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Dafne D. G. Horovitz
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Carolina Fischinger Moura de Souza
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Ida V. D. Schwartz
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Andrew Green
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Mohammed Al-Owain
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Graciella Uziel
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Sabine Sigaudy
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Brigitte Chabrol
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Franc-Jan van Spronsen
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Martin Steinert
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Eleni Komini
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Donald Wurm
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Andrea Bevot
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Addelkarim Ayadi
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Karin Huijben
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Marli Dercksen
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Peter Witters
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Jaak Jaeken
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Gert Matthijs
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Dirk J. Lefeber
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Ron A. Wevers
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Corresponding authors

Correspondence to Eva Morava or Ron A. Wevers.

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The online version of the original article can be found at http://dx.doi.org/10.1007/s10545-016-9945-x.

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Morava, E., Tiemes, V., Thiel, C. et al. Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. J Inherit Metab Dis 39, 759 (2016). https://doi.org/10.1007/s10545-016-9967-4

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Published: 08 August 2016
Issue Date: September 2016
DOI: https://doi.org/10.1007/s10545-016-9967-4

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Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

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