Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies (J Inherit Metab Dis, 10.1007/s10545-016-9945-x)

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

Research output: Contribution to journalComment/debate

Abstract

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

Original languageEnglish (US)
Pages (from-to)759
Number of pages1
JournalJournal of inherited metabolic disease
Volume39
Issue number5
DOIs
StatePublished - Sep 1 2016

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Morava, E., Tiemes, V., Thiel, C., Seta, N., de Lonlay, P., de Klerk, H., Mulder, M., Rubio-Gozalbo, E., Visser, G., van Hasselt, P., Horovitz, D. D. G., de Souza, C. F. M., Schwartz, I. V. D., Green, A., Al-Owain, M., Uziel, G., Sigaudy, S., Chabrol, B., van Spronsen, F. J., ... Wevers, R. A. (2016). Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies (J Inherit Metab Dis, 10.1007/s10545-016-9945-x). Journal of inherited metabolic disease, 39(5), 759. https://doi.org/10.1007/s10545-016-9967-4