ALG6-CDG: a recognizable phenotype with epilepsy, proximal...

Journal of Inherited Metabolic Disease 2016 / 9 Vol. 39; Iss. 5

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

Morava, Eva, Tiemes, Vera, Tiel, Christian, Seta, Nathalie, de Lonlay, Pascale, de Klerk, Hans, Mulder, Margot, Rubio-Gozalbo, Estela, Visser, Gepke, van Hasselt, Peter, Horovitz, Dafne D. G., de Souz
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Volume:
39
Language:
english
Journal:
Journal of Inherited Metabolic Disease
DOI:
10.1007/s10545-016-9945-x
Date:
September, 2016
File:
PDF, 505 KB
english, 2016
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