Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

dc.contributor.author	Valdés Mas, Rafael María
dc.contributor.author	Gutiérrez Fernández, Ana Yolanda
dc.contributor.author	Gómez de Oña, Juan
dc.contributor.author	Coto García, Eliecer
dc.contributor.author	Astudillo González, María Aurora
dc.contributor.author	Álvarez Puente, Diana
dc.contributor.author	Rodríguez Reguero, José Julián
dc.date.accessioned	2015-03-20T12:41:28Z
dc.date.available	2015-03-20T12:41:28Z
dc.date.issued	2014
dc.identifier.citation	Nature Communications, 5:5326 (2014); doi:10.1038/ncomms6326
dc.identifier.issn	2041-1723
dc.identifier.uri	http://hdl.handle.net/10651/30366
dc.description.sponsorship	Ministerio de Economia y Competitividad-Spain; Fundacion Botin; Instituto de Salud Carlos III-Fondo Europeo de Desarrollo Regional [FIS-12/00287]; Obra Social Cajastur; Instituto de Salud Carlos III (RTICC)
dc.format.extent	5326
dc.language.iso	eng
dc.relation.ispartof	Nature Communications
dc.rights	© 2014 Macmillan Publishers Limited. All rights reserved.
dc.rights	CC Reconocimiento - No comercial - Sin obras derivadas 4.0 Internacional
dc.rights.uri	http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.source	WOS:000344062100002
dc.title	Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
dc.type	journal article
dc.identifier.doi	10.1038/ncomms6326
dc.relation.projectID	MINECO
dc.relation.projectID	FEDER/FIS-12/00287
dc.relation.publisherversion	http://dx.doi.org/10.1038/ncomms6326
dc.rights.accessRights	open access

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