Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcó, A Pujol, C Roca, S Motas… - Disease models & …, 2016 - journals.biologists.com
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …
被引用次数：28 相关文章
[PDF] cyberleninka.org

[PDF][PDF] Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcó, A Pujol, C Roca, S Motas, A Ribera, M Garcia… - 2016 - cyberleninka.org
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …
[PDF] academia.edu

[PDF][PDF] Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcó, A Pujol, C Roca, S Motas, A Ribera, M Garcia… - 2016 - academia.edu
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …

Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcò, A Pujol, C Roca, S Motas… - DMM Disease …, 2016 - portalrecerca.uab.cat
Abstract© 2016. Published by The Company of Biologists Ltd. Mucopolysaccharidosis type
IIIC (MPSIIIC) is a severe lysosomal storage disease causedbydeficiency inactivityofthe …
[PDF] core.ac.uk

[PDF][PDF] Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcó, A Pujol, C Roca, S Motas, A Ribera, M Garcia… - 2016 - core.ac.uk
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …

Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcó, A Pujol, C Roca, S Motas… - Disease models & …, 2016 - pubmed.ncbi.nlm.nih.gov
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …

Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC.

S Marcó, A Pujol, C Roca, S Motas… - Disease Models & …, 2016 - europepmc.org
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …
[HTML] nih.gov

[HTML][HTML] Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcó, A Pujol, C Roca, S Motas… - Disease Models & …, 2016 - ncbi.nlm.nih.gov
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …

Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcó, A Pujol, C Roca, S Motas… - Disease Models & …, 2016 - search.proquest.com
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …

Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC

S Marcó, A Pujol i Altarriba, C Roca, S Motas… - Disease Models & …, 2016 - ddd.uab.cat
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe lysosomal storage disease caused by
deficiency in activity of the transmembrane enzyme heparan-α-glucosaminide N …