Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

dc.contributor.author	Carracedo Álvarez, Ángel
dc.contributor.author	Brión Martínez, María José
dc.contributor.author	Blanco Verea, Alejandro José
dc.contributor.author	Sobrino Rey, Beatríz
dc.contributor.author	Amigo Lechuga, Jorge
dc.contributor.author	Gago Díaz, Marina
dc.date.accessioned	2017-06-07T07:16:32Z
dc.date.available	2017-06-07T07:16:32Z
dc.date.issued	2014
dc.identifier.issn	0009-8981
dc.identifier.uri	http://hdl.handle.net/20.500.11940/4606
dc.language.iso	eng
dc.title	Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease
dc.type	Artigo	es
dc.authorsophos	Gago-Díaz, M.
dc.authorsophos	Blanco-Verea, A.
dc.authorsophos	Teixidó-Turà, G.
dc.authorsophos	Valenzuela, I.
dc.authorsophos	Del Campo, M.
dc.authorsophos	Borregan, M.
dc.authorsophos	Sobrino, B.
dc.authorsophos	Amigo, J.
dc.authorsophos	García-Dorado, D.
dc.authorsophos	Evangelista, A.
dc.authorsophos	Carracedo, A.
dc.authorsophos	Brion, M.
dc.identifier.doi	10.1016/j.cca.2014.07.016
dc.identifier.isi	342246900016
dc.identifier.pmid	25046559
dc.identifier.sophos	14677
dc.issue.number	437
dc.journal.title	CLINICA CHIMICA ACTA
dc.organization	Consellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago::IDIS.- Instituto de investigaciones sanitarias de Santiago
dc.page.initial	88
dc.page.final	92
dc.rights.accessRights	openAccess
dc.typesophos	Artículo Original
dc.volume.number	437

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