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	1.	Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. [electronic resource] by 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 Wevers, Ron A Publication details: Journal of inherited metabolic disease 09 2016 In: Journal of inherited metabolic disease vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. [electronic resource] by 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 Wevers, Ron A Producer: 20171206 In: Journal of inherited metabolic disease vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)