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Pesquisa de variantes genéticas causadoras de cardiomiopatia hipertrófica familiar através de painel multi-genes

dc.contributor.authorCamargo, Amanda Cristofolipt_BR
dc.contributor.authorScolari, Fernando Luíspt_BR
dc.contributor.authorSiebert, Marinapt_BR
dc.contributor.authorMatte, Ursula da Silveirapt_BR
dc.contributor.authorVairo, Filippo Pinto ept_BR
dc.contributor.authorMattos, Beatriz Piva ept_BR
dc.date.accessioned2021-11-19T04:57:33Zpt_BR
dc.date.issued2020pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/232051pt_BR
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoporpt_BR
dc.relation.ispartofClinical and biomedical research. Porto Alegrept_BR
dc.rightsOpen Accessen
dc.subjectGenéticapt_BR
dc.titlePesquisa de variantes genéticas causadoras de cardiomiopatia hipertrófica familiar através de painel multi-genespt_BR
dc.title.alternativePesquisa de variantes genéticas causadoras de cardiomiopatia hipertrófica familiar através de painel multigenes pt
dc.typeResumo publicado em eventopt_BR
dc.contributor.eventHospital de Clínicas de Porto Alegre. Semana Científica. (40. : 2020 : Porto Alegre, RS)pt_BR
dc.identifier.nrb001133156pt_BR
dc.type.originNacionalpt_BR


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