Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies (vol 39, pg 713, 2016)
Files
Publication date
2016-09
Authors
Morava, Eva
Tiemes, Vera
Thiel, Christian
Seta, Nathalie
de Lonlay, Pascale
de Klerk, Hans
Mulder, Margot
Rubio-Gozalbo, Estela
Visser, Gepke
van Hasselt, Peter
Editors
Advisors
Supervisors
Document Type
Comment
Metadata
Show full item recordCollections
License
taverne
Abstract
Keywords
Taverne, Published Erratum
Citation
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, Komini, E, Wurm, D, Bevot, A, Ayadi, A, Huijben, K, Dercksen, M, Witters, P, Jaeken, J, Matthijs, G, Lefeber, D 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, vol. 39, no. 5, pp. 759-759. https://doi.org/10.1007/s10545-016-9967-4