Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies (vol 39, pg 713, 2016)

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 Steinert; Eleni Komini; Donald Wurm; Andrea Bevot; Addelkarim Ayadi; Karin Huijben; Marli Dercksen; Peter Witters; Jaak Jaeken; Gert Matthijs; Dirk J. Lefeber; Ron A. Wevers

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 (vol 39, pg 713, 2016)

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 journal › Comment/Letter to the editor › Academic › peer-review

Original language	English
Pages (from-to)	759-759
Journal	Journal of Inherited Metabolic Disease
Volume	39
Issue number	5
DOIs	https://doi.org/10.1007/s10545-016-9967-4
Publication status	Published - Sept 2016

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10.1007/s10545-016-9967-4

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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., Moura de Souza, C. F., 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 (vol 39, pg 713, 2016). Journal of Inherited Metabolic Disease, 39(5), 759-759. https://doi.org/10.1007/s10545-016-9967-4

@article{c1f8f141812a4edd8e90273344f9fa65,

title = "Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies (vol 39, pg 713, 2016)",

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

year = "2016",

month = sep,

doi = "10.1007/s10545-016-9967-4",

language = "English",

volume = "39",

pages = "759--759",

journal = "Journal of Inherited Metabolic Disease",

issn = "0141-8955",

publisher = "Springer Netherlands",

number = "5",

}

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, DDG, Moura de Souza, CF, Schwartz, IVD, Green, A, Al-Owain, M, Uziel, G, Sigaudy, S, Chabrol, B, van Spronsen, F-J, Steinert, M, Komini, E, Wurm, D, Bevot, A, Ayadi, A, Huijben, K, Dercksen, M, Witters, P, Jaeken, J, Matthijs, G, Lefeber, DJ & Wevers, RA 2016, 'Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies (vol 39, pg 713, 2016)', Journal of Inherited Metabolic Disease, vol. 39, no. 5, pp. 759-759. https://doi.org/10.1007/s10545-016-9967-4

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies (vol 39, pg 713, 2016). / Morava, Eva; Tiemes, Vera; Thiel, Christian et al.
In: Journal of Inherited Metabolic Disease, Vol. 39, No. 5, 09.2016, p. 759-759.

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

TY - JOUR

T1 - Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies (vol 39, pg 713, 2016)

AU - Morava, Eva

AU - Tiemes, Vera

AU - Thiel, Christian

AU - Seta, Nathalie

AU - de Lonlay, Pascale

AU - de Klerk, Hans

AU - Mulder, Margot

AU - Rubio-Gozalbo, Estela

AU - Visser, Gepke

AU - van Hasselt, Peter

AU - Horovitz, Dafne D. G.

AU - Moura de Souza, Carolina Fischinger

AU - Schwartz, Ida V. D.

AU - Green, Andrew

AU - Al-Owain, Mohammed

AU - Uziel, Graciella

AU - Sigaudy, Sabine

AU - Chabrol, Brigitte

AU - van Spronsen, Franc-Jan

AU - Steinert, Martin

AU - Komini, Eleni

AU - Wurm, Donald

AU - Bevot, Andrea

AU - Ayadi, Addelkarim

AU - Huijben, Karin

AU - Dercksen, Marli

AU - Witters, Peter

AU - Jaeken, Jaak

AU - Matthijs, Gert

AU - Lefeber, Dirk J.

AU - Wevers, Ron A.

PY - 2016/9

Y1 - 2016/9

U2 - 10.1007/s10545-016-9967-4

DO - 10.1007/s10545-016-9967-4

M3 - Comment/Letter to the editor

C2 - 27498540

SN - 0141-8955

VL - 39

SP - 759

EP - 759

JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

IS - 5

ER -