TY  - JOUR 
AU  - Álvarez González, José Victor
AU  - Bravo López, Susana Belén
AU  - García-Vence, M.
AU  - De Castro López, María José
AU  - Luzardo, A.
AU  - Colón Mejeras, Cristobal
AU  - Tomatsu, S.
AU  - Otero Espinar, Francisco
AU  - Couce Pico,  María Luz
PY  - 2019
SN  - 1661-6596
UR  - http://hdl.handle.net/20.500.11940/15803
AB  - Morquio A syndrome, or mucopolysaccharidosis type IVA (MPS IVA), is a lysosomal storage disease due to mutations in the N-acetylgalactosamine-6-sulfatase (GALNS) gene. Systemic skeletal dysplasia and the related clinical features of MPS IVA are due to...
LA  - eng
KW  - Adult
KW  - Humans
KW  - Chondroitinsulfatases
KW  - Young Adult
KW  - Cells
KW  - Drug Delivery Systems
KW  - Liposomes
KW  - Enzyme Replacement Therapy
KW  - Proteomics
KW  - Lipids
KW  - Nanostructures
KW  - Mucopolysaccharidosis IV
TI  - Proteomic analysis in morquio a cells treated with immobilized enzymatic replacement therapy on nanostructured lipid systems
DO  - 10.3390/ijms20184610
T2  - INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
M2  - 4610
KW  - CHUS
KW  - IDIS
VL  - 20
ER  -