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dc.contributor.authorCarracedo Álvarez, Ángel
dc.contributor.authorBlanco Arias, Patricia
dc.contributor.authorArias Gómez, Manuel 
dc.contributor.authorPardo Fernández, Julio 
dc.contributor.authorGuijarro del Amo, Mónica 
dc.date.accessioned2017-06-07T07:26:14Z
dc.date.available2017-06-07T07:26:14Z
dc.date.issued2011
dc.identifier.issn0960-8966
dc.identifier.urihttp://hdl.handle.net/20.500.11940/6416
dc.titleP3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K)
dc.typePublicación de congreso
dc.authorsophosGuijarro, M.
dc.authorsophosBlanco-Arias, P.
dc.authorsophosPardo, J.
dc.authorsophosConcheiro-Álvarez, C.
dc.authorsophosSan Millán, B.
dc.authorsophosJoglar-Santos, J.
dc.authorsophosArias-Gómez, M.
dc.authorsophosNavarro Fernández-Balbuena, C.
dc.authorsophosCarracedo Álvarez, A.
dc.authorsophosSobrido, M.
dc.identifier.doi10.1016/j.nmd.2011.06.917
dc.identifier.isi295955900166
dc.identifier.sophos10723
dc.issue.number42652
dc.journal.titleNEUROMUSCULAR DISORDERS
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Neuroloxía
dc.page.initial688
dc.page.final689
dc.rights.accessRightsopenAccess
dc.typesophosComunicaciones a congresos
dc.volume.number21


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