PRKG1 mutations and thoracic aortic disease: Another candidate gene to consider during genetic diagnosis approach to non-syndromic cases

dc.contributor.author	Brión Martínez, María José
dc.contributor.author	Blanco Verea, Alejandro José
dc.contributor.author	Gago Díaz, Marina
dc.date.accessioned	2017-06-07T07:17:47Z
dc.date.available	2017-06-07T07:17:47Z
dc.date.issued	2015
dc.identifier.issn	0195-668X
dc.identifier.uri	http://hdl.handle.net/20.500.11940/4810
dc.language.iso	eng
dc.title	PRKG1 mutations and thoracic aortic disease: Another candidate gene to consider during genetic diagnosis approach to non-syndromic cases
dc.type	Publicación de congreso
dc.authorsophos	Gago-Diaz, M.
dc.authorsophos	Blanco-Verea, A.
dc.authorsophos	Teixido, G.
dc.authorsophos	Huguet, F.
dc.authorsophos	Carracedo, A.
dc.authorsophos	Evangelista, A.
dc.authorsophos	Brion, M.
dc.identifier.sophos	18978
dc.journal.title	European Heart Journal
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago::IDIS.- Instituto de investigaciones sanitarias de Santiago
dc.page.initial	529
dc.page.final	530
dc.rights.accessRights	openAccess
dc.typesophos	Comunicaciones a congresos
dc.volume.number	36

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