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dc.contributor | Universitat de Barcelona |
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dc.contributor.author | Matos, Liliana |
dc.contributor.author | Canals Montferrer, Isaac |
dc.contributor.author | Dridi, Larbi |
dc.contributor.author | Choi, Yoo |
dc.contributor.author | Prata, Maria Joao |
dc.contributor.author | Jordan, Peter |
dc.contributor.author | Desviat, Lourdes R. |
dc.contributor.author | Pérez, Belén |
dc.contributor.author | Pshezhetsky, Alexey V. |
dc.contributor.author | Grinberg Vaisman, Daniel Raúl |
dc.contributor.author | Alves, Sandra |
dc.contributor.author | Vilageliu i Arqués, Lluïsa |
dc.date | 2015-09-01T12:28:26Z |
dc.date | 2015-09-01T12:28:26Z |
dc.date | 2014-12-24 |
dc.date | 2015-09-01T12:28:26Z |
dc.identifier.citation | 1750-1172 |
dc.identifier.citation | 647725 |
dc.identifier.uri | http://hdl.handle.net/2445/66803 |
dc.format | 12 p. |
dc.format | application/pdf |
dc.language.iso | eng |
dc.publisher | BioMed Central |
dc.relation | Reproducció del document publicat a: http://dx.doi.org/10.1186/s13023-014-0180-y |
dc.relation | Orphanet Journal of Rare Diseases, 2014, vol. 9, num. 180 |
dc.relation | http://dx.doi.org/10.1186/s13023-014-0180-y |
dc.rights | cc-by (c) Matos, L. et al., 2014 |
dc.rights | info:eu-repo/semantics/openAccess |
dc.rights | http://creativecommons.org/licenses/by/3.0/es |
dc.subject | Mutació (Biologia) |
dc.subject | Lisosomes |
dc.subject | Mutation (Biology) |
dc.subject | Lysosomes |
dc.title | Therapeutic strategies based on modified U1 snRNAs and chaperones for Sanfilippo C splicing mutations |
dc.type | info:eu-repo/semantics/article |
dc.type | info:eu-repo/semantics/publishedVersion |
dc.description.abstract |