APA (7th ed.) Citation

Morava-Kozicz, E., Tiemes, V., Thiel, C., Seta, N., Lonlay, P. d., Klerk, H. d., . . . Wevers, R. A. (2016). ALG6-CDG: A recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. Journal of inherited metabolic disease, 39(5), . https://doi.org/10.1007/s10545-016-9945-x

Chicago Style (17th ed.) Citation

Morava-Kozicz, Eva, et al. "ALG6-CDG: A Recognizable Phenotype with Epilepsy, Proximal Muscle Weakness, Ataxia and Behavioral and Limb Anomalies." Journal of Inherited Metabolic Disease 39, no. 5 (2016). https://doi.org/10.1007/s10545-016-9945-x.

MLA (9th ed.) Citation

Morava-Kozicz, Eva, et al. "ALG6-CDG: A Recognizable Phenotype with Epilepsy, Proximal Muscle Weakness, Ataxia and Behavioral and Limb Anomalies." Journal of Inherited Metabolic Disease, vol. 39, no. 5, 2016, https://doi.org/10.1007/s10545-016-9945-x.