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)

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

Additional Metadata
Persistent URL	doi.org/10.1007/s10545-016-9967-4, hdl.handle.net/1765/93380
Journal	Journal of Inherited Metabolic Disease
Organisation	Department of Pediatrics
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	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., Schwartz, I., Green, A., Al-Owain, M., Uziel, G., Sigaudy, S., Chabrol, B., van Spronsen, F.-J., … Wevers, R. (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).https://doi.org/10.1007/s10545-016-9967-4

See Also
article ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies E. Morava (Eva), V. Tiemes (Vera), C. Thiel (Christian), N. Seta (Nathalie), P. de Lonlay (Pascale), H. de Klerk, M.F. Mulder (Margot), M.E. Rubio-Gozalbo (Estela), G. Visser (G.), P.M. van Hasselt (Peter), et al. J. Jaeken, R.A. Wevers (Ron)

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