Congenital myasthenia and congenital disorders of glycosylation caused by mutations in the DPAGT1 gene

Publication date: Available online 28 January 2019Source: Neurología (English Edition)Author(s): S. Ibáñez-Micó, R. Domingo Jiménez, C. Pérez-Cerdá, D. Ghandour-Fabre

Source: Neurologia - January 29, 2019 Category: Neurology Source Type: research