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Letter to the Editor
Congenital myasthenia and congenital disorders of glycosylation caused by mutations in the DPAGT1 gene
Miastenia congénita y defecto congénito de la glucosilación por mutaciones en el gen DPAGT1
S. Ibáñez-Micóa,
Corresponding author
, R. Domingo Jiméneza, C. Pérez-Cerdáb, D. Ghandour-Fabrea
a Sección de Neuropediatría, Servicio de Pediatría, Hospital Virgen de la Arrixaca, Murcia, Spain
b Centro de Diagnóstico de Enfermedades Moleculares (CEDEM), Universidad Autónoma de Madrid, Madrid, Spain
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ISSN: 21735808
Original language: English
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