Minimal symptoms in McArdle disease: A real PYGM genotype effect?

dc.contributor.authorPinós, Tomás
dc.contributor.authorLucía Mulas, Alejandro
dc.contributor.authorArenas, Joaquín
dc.contributor.authorBrull, Astrid
dc.contributor.authorMartín, Miguel Ángel
dc.contributor.authorNogales-Gadea, Gisela
dc.date.accessioned2016-02-19T11:31:32Z
dc.date.available2016-02-19T11:31:32Z
dc.date.issued2015
dc.description.filiationUEMspa
dc.description.impact2.713 JCR (2015) Q2, 73/192 Clinical neurology, 123/256 Neurosciencesspa
dc.description.sponsorshipSin financiaciónspa
dc.identifier.citationPinós, T., Lucía, A., Arenas, J., Brull, A., Andreu, A. L., Martín, M. Á., & Nogales‐Gadea, G. (2015). Minimal symptoms in McArdle disease: A real PYGM genotype effect?. Muscle & nerve, 52(6), 1136-1137.spa
dc.identifier.doi10.1002/mus.24789
dc.identifier.issn0148639X
dc.identifier.issn10974598
dc.identifier.urihttp://hdl.handle.net/11268/4914
dc.language.isoengspa
dc.peerreviewedSispa
dc.rights.accessRightsrestricted accessspa
dc.subject.uemEnfermedades - McArdlespa
dc.subject.unescoEnfermedadspa
dc.subject.unescoMedicinaspa
dc.titleMinimal symptoms in McArdle disease: A real PYGM genotype effect?spa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublicationd3691359-d7bd-4a12-b84e-338e28c81f9f
relation.isAuthorOfPublication.latestForDiscoveryd3691359-d7bd-4a12-b84e-338e28c81f9f

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