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iPSCs disease models and CRISPR/Cas9 editing: the basics

dc.contributor.authorAmaral, Olga
dc.date.accessioned2020-06-01T18:44:41Z
dc.date.available2020-06-01T18:44:41Z
dc.date.issued2019-10
dc.descriptionInvited speaker
dc.description.abstractInvited speaker at Med-Lysosomal2019. Following the success of three earlier meetings on rare diseases wherein LSDs were important components, the meeting in London focused on the diagnosis and treatment as well as on new therapeutic modalities already in advanced stages of development of four main Lysosomal Diseases: Gaucher, Fabry, Pompe and MPSs.pt_PT
dc.description.sponsorshipOA received funding from FCT grant PTDC/BIM-MEC/4762/2014pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/6892
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.relation.publisherversionhttps://www.med-lysosomal.com/pt_PT
dc.subjectHuman Geneticspt_PT
dc.subjectGene Editingpt_PT
dc.subjectCRISPR/Caspt_PT
dc.subjectCell Modelspt_PT
dc.subjectDoenças Genéticaspt_PT
dc.titleiPSCs disease models and CRISPR/Cas9 editing: the basicspt_PT
dc.typelecture
dspace.entity.typePublication
oaire.citation.conferencePlaceLondon, UKpt_PT
oaire.citation.titleThe European Conference on Recent Advances in Lysosomal Diseases (Med-Lysosomal), 24-25 October 2019pt_PT
rcaap.rightsclosedAccesspt_PT
rcaap.typelecturept_PT

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