Publicação
Development of a U1 snRNA-adapted gene therapeutic strategy to correct 5’ splicing defects in lysosomal storage disorders
| dc.contributor.author | Matos, Liliana | |
| dc.contributor.author | Alves, Sandra | |
| dc.date.accessioned | 2016-03-03T18:15:20Z | |
| dc.date.available | 2016-05-01T00:30:11Z | |
| dc.date.issued | 2015-03-19 | |
| dc.description.sponsorship | LM was supported by a Grant (SFRH/BD/64592/2009) | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.18/3607 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.subject | Doenças Genéticas | pt_PT |
| dc.subject | U1snRNA therapy | pt_PT |
| dc.subject | Lysosomal Storage Disorders | pt_PT |
| dc.subject | MPS III C | pt_PT |
| dc.subject | ML III alpha/beta | pt_PT |
| dc.subject | MPS I | pt_PT |
| dc.title | Development of a U1 snRNA-adapted gene therapeutic strategy to correct 5’ splicing defects in lysosomal storage disorders | pt_PT |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.citation.conferencePlace | Porto, Portugal | pt_PT |
| oaire.citation.title | 11th International Symposium SPDM, 19 março 2015 | pt_PT |
| rcaap.rights | restrictedAccess | pt_PT |
| rcaap.type | conferenceObject | pt_PT |
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