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

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^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

1 Erratum / corrigendum

1 results

2016

Erratum to: ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies
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. & Steinert, M. & 11 others, Komini, E., Wurm, D., Bevot, A., Ayadi, A., Huijben, K., Dercksen, M., Witters, P., Jaeken, J., Matthijs, G., Lefeber, D. J. & Wevers, R. A., Sept 2016, In: Journal of Inherited Metabolic Disease. 39, 5, p. 759-759
Research output: Contribution to journal › Erratum / corrigendum › Academic

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

Research output

Search results

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