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

dc.contributor.author	Ibáñez-Mico, Salvador
dc.contributor.author	Domingo-Jiménez, Rosario
dc.contributor.author	Pérez-Cerdá, C
dc.contributor.author	Ghandour-Fabre, D
dc.date.accessioned	2026-02-12T12:05:55Z
dc.date.available	2026-02-12T12:05:55Z
dc.date.issued	2019-03
dc.identifier.citation	Ibáñez-Micó S, Domingo Jiménez R, Pérez-Cerdá C, Ghandour-Fabre D. Miastenia congénita y defecto congénito de la glucosilación por mutaciones en el gen DPAGT1. Neurología. marzo de 2019;34(2):139-41.
dc.identifier.issn	0213-4853
dc.identifier.uri	https://sms.carm.es/ricsmur/handle/123456789/24217
dc.language.iso	spa
dc.publisher	ELSEVIER ESPANA SLU
dc.rights	Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internaciona
dc.rights.uri	http://creativecommons.org/licenses/by-nc-nd/4.0/	*
dc.title	Congenital myasthenia and congenital disorders of glycosylation caused by mutations in the DPAGT1 gene
dc.type	info:eu-repo/semantics/article
dc.identifier.pmid	28712839
dc.relation.publisherversion	https://linkinghub.elsevier.com/retrieve/pii/S0213485317302153
dc.type.version	info:eu-repo/semantics/publishedVersion
dc.identifier.doi	10.1016/j.nrl.2017.05.002
dc.journal.title	Neurología
dc.identifier.essn	1578-1968