High prevalence of N271I founder mutation in TNNT2 gene detected by NGS in a galician cohort cause hypertrophic cardiomyopathy associated with a benign course

dc.contributor.author	Monserrat Iglesias, Lorenzo
dc.contributor.author	Fernández Fernández, Xusto
dc.contributor.author	Barriales Villa, Roberto
dc.contributor.author	Ortiz Genga, Martín
dc.date.accessioned	2017-06-07T07:09:39Z
dc.date.available	2017-06-07T07:09:39Z
dc.date.issued	2015
dc.identifier.issn	0195-668X
dc.identifier.uri	http://hdl.handle.net/20.500.11940/3277
dc.language.iso	eng
dc.title	High prevalence of N271I founder mutation in TNNT2 gene detected by NGS in a galician cohort cause hypertrophic cardiomyopathy associated with a benign course
dc.type	Publicación de congreso
dc.authorsophos	Ochoa, J. P.
dc.authorsophos	Barriales Villa, R.
dc.authorsophos	Pena, M. L.
dc.authorsophos	Palomino Doza, J.
dc.authorsophos	Ortiz Genga, M.
dc.authorsophos	Alonso Garcia, D.
dc.authorsophos	Fernandez Fernandez, X.
dc.authorsophos	Monserrat Iglesias, L.
dc.identifier.sophos	18156
dc.journal.title	European Heart Journal
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña::INIBIC.- Instituto de Investigación Biomédica
dc.page.initial	271
dc.page.final	272
dc.rights.accessRights	openAccess
dc.typesophos	Comunicaciones a congresos
dc.volume.number	36

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