Publication
Lysosomal Storage Diseases: an overview
| dc.contributor.author | Alves, Sandra | |
| dc.date.accessioned | 2019-03-25T16:05:54Z | |
| dc.date.available | 2019-03-25T16:05:54Z | |
| dc.date.issued | 2018-10-29 | |
| dc.description.abstract | Lysosomal storage diseases (LSDs)are an heterogenous group rare inherited metabolic diseases caused by mutations mutations in proteins critical critical for lysosomal function. | pt_PT |
| dc.description.sponsorship | FCT PTDC/BIM-MEC/4762/2014 | pt_PT |
| dc.description.version | N/A | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.18/6298 | |
| dc.language.iso | eng | pt_PT |
| dc.subject | Lysosomal Storage Diseases | pt_PT |
| dc.subject | Rare Inherited Metabolic Diseases | pt_PT |
| dc.subject | Doenças Genéticas | pt_PT |
| dc.subject | Genética Humana | pt_PT |
| dc.title | Lysosomal Storage Diseases: an overview | pt_PT |
| dc.type | lecture | |
| dspace.entity.type | Publication | |
| oaire.citation.conferencePlace | Porto, Portugal | pt_PT |
| oaire.citation.title | Iniciativa "À volta da investigação”- uma manhã à volta da investigação em doenças genéticas, no âmbito do projeto “Cemoly- cell models for lysosomal disorders, INSA, 29 outubro 2018 | pt_PT |
| rcaap.rights | restrictedAccess | pt_PT |
| rcaap.type | lecture | pt_PT |
