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Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C

dc.contributor.authorReinstein, E.
dc.contributor.authorGutiérrez Fernández, Ana Yolanda 
dc.contributor.authorTzur, S.
dc.contributor.authorBormans, C.
dc.contributor.authorMarcu, S.
dc.contributor.authorTayeb-Fligelman, E.
dc.contributor.authorVinkler, C.
dc.contributor.authorRaas-Rothschild, A.
dc.contributor.authorIrge, D.
dc.contributor.authorLandau, M.
dc.contributor.authorShohat, M.
dc.contributor.authorSuárez Puente, Xosé Antón 
dc.contributor.authorBehar, D. M.
dc.contributor.authorLópez Otín, Carlos 
dc.date.accessioned2017-02-22T10:34:43Z
dc.date.available2017-02-22T10:34:43Z
dc.date.issued2016
dc.identifier.citationEuropean Journal of Human Genetics, 24, p. 1792–1796 (2016); doi:10.1038/ejhg.2016.110
dc.identifier.issn1018-4813
dc.identifier.urihttp://hdl.handle.net/10651/40508
dc.description.sponsorshipWe thank Rabin Medical Center and Adler cathedra for pediatric cardiology for the support. This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors
dc.format.extentp. 1792–1796
dc.language.isoeng
dc.relation.ispartofEuropean Journal of Human Genetics
dc.rights©,
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84986540256&partnerID=40&md5=deb7840f903e2cc95de5421788edf60e
dc.titleCongenital dilated cardiomyopathy caused by biallelic mutations in Filamin C
dc.typejournal article
dc.identifier.doi10.1038/ejhg.2016.110
dc.relation.publisherversionhttp://dx.doi.org/10.1038/ejhg.2016.110


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