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 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 (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

Medical Genetics

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

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

Original language	English (US)
Pages (from-to)	759
Number of pages	1
Journal	Journal of inherited metabolic disease
Volume	39
Issue number	5
DOIs	https://doi.org/10.1007/s10545-016-9967-4
State	Published - Sep 1 2016

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Access to Document

10.1007/s10545-016-9967-4

Cite this

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

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). / Morava, Eva; Tiemes, Vera; Thiel, Christian et al.
In: Journal of inherited metabolic disease, Vol. 39, No. 5, 01.09.2016, p. 759.

Research output: Contribution to journal › Comment/debate › peer-review

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, de Souza, CFM, Schwartz, IVD, Green, A, Al-Owain, M, Uziel, G, Sigaudy, S, Chabrol, B, van Spronsen, FJ, 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 (J Inherit Metab Dis, 10.1007/s10545-016-9945-x)', Journal of inherited metabolic disease, vol. 39, no. 5, pp. 759. https://doi.org/10.1007/s10545-016-9967-4

@article{465f32939d2d436fa3cb6789d3c5baf3,

title = "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)",

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

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 {de Souza}, {Carolina Fischinger Moura} 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.}",

note = "Publisher Copyright: {\textcopyright} 2016, Springer-Verlag Berlin Heidelberg.",

year = "2016",

month = sep,

day = "1",

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

language = "English (US)",

volume = "39",

pages = "759",

journal = "Journal of inherited metabolic disease",

issn = "0141-8955",

publisher = "Springer Netherlands",

number = "5",

}

TY - JOUR

T1 - Erratum to

T2 - 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)

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 - de Souza, Carolina Fischinger Moura

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 - 2016/9/1

Y1 - 2016/9/1

N2 - The name of the author Christian Thiel was rendered wrongly in the original publication but has since been corrected.

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

UR - http://www.scopus.com/inward/record.url?scp=84988240451&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84988240451&partnerID=8YFLogxK

U2 - 10.1007/s10545-016-9967-4

DO - 10.1007/s10545-016-9967-4

M3 - Comment/debate

AN - SCOPUS:84988240451

SN - 0141-8955

VL - 39

SP - 759

JO - Journal of inherited metabolic disease

JF - Journal of inherited metabolic disease

IS - 5

ER -

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)

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this