APA
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., 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. (092016). Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. : Journal of inherited metabolic disease.
Chicago
Morava Eva, Tiemes Vera, Thiel Christian, Seta Nathalie, de Lonlay Pascale, de Klerk Hans, Mulder Margot, Rubio-Gozalbo Estela, Visser Gepke, van Hasselt Peter, Horovitz Dafne D G, de Souza Carolina Fischinger Moura, Schwartz Ida V D, Green Andrew, Al-Owain Mohammed, Uziel Graciella, Sigaudy Sabine, Chabrol Brigitte, van Spronsen Franc-Jan, Steinert Martin, Komini Eleni, Wurm Donald, Bevot Andrea, Ayadi Addelkarim, Huijben Karin, Dercksen Marli, Witters Peter, Jaeken Jaak, Matthijs Gert, Lefeber Dirk J and Wevers Ron A. 092016. Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. : Journal of inherited metabolic disease.
Harvard
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., Steinert M., Komini E., Wurm D., Bevot A., Ayadi A., Huijben K., Dercksen M., Witters P., Jaeken J., Matthijs G., Lefeber D. J. and Wevers R. A. (092016). Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. : Journal of inherited metabolic disease.
MLA
Morava Eva, Tiemes Vera, Thiel Christian, Seta Nathalie, de Lonlay Pascale, de Klerk Hans, Mulder Margot, Rubio-Gozalbo Estela, Visser Gepke, van Hasselt Peter, Horovitz Dafne D G, de Souza Carolina Fischinger Moura, Schwartz Ida V D, Green Andrew, Al-Owain Mohammed, Uziel Graciella, Sigaudy Sabine, Chabrol Brigitte, van Spronsen Franc-Jan, Steinert Martin, Komini Eleni, Wurm Donald, Bevot Andrea, Ayadi Addelkarim, Huijben Karin, Dercksen Marli, Witters Peter, Jaeken Jaak, Matthijs Gert, Lefeber Dirk J and Wevers Ron A. Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. : Journal of inherited metabolic disease. 092016.