[HTML][HTML] Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II
HFE Gleitz, C O'Leary, RJ Holley, BW Bigger - PLoS One, 2017 - journals.plos.org
Severe mucopolysaccharidosis type II (MPS II) is a progressive lysosomal storage disease
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II
HFE Gleitz, C O'Leary, RJ Holley, BW Bigger - PloS one, 2017 - pubmed.ncbi.nlm.nih.gov
Severe mucopolysaccharidosis type II (MPS II) is a progressive lysosomal storage disease
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
Identification of Age-Dependent Motor and Neuropsychological Behavioural Abnormalities in a Mouse Model of Mucopolysaccharidosis Type II
H Gleitz, C O'Leary, R Holley, B Bigger - PLoS ONE, 2017 - research.manchester.ac.uk
Severe mucopolysaccharidosis type II (MPS II) is a progressive lysosomal storage disease
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
[引用][C] Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II
HFE Gleitz, C O'Leary, RJ Holley, BW Bigger - PLoS ONE, 2017 - ui.adsabs.harvard.edu
Identification of age-dependent motor and neuropsychological behavioural abnormalities in
a mouse model of Mucopolysaccharidosis Type II - NASA/ADS Now on home page ads icon …
a mouse model of Mucopolysaccharidosis Type II - NASA/ADS Now on home page ads icon …
[PDF][PDF] Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II
HFE Gleitz, C O'Leary, RJ Holley, BW Bigger - PLoS ONE, 2017 - pdfs.semanticscholar.org
Severe mucopolysaccharidosis type II (MPS II) is a progressive lysosomal storage disease
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
[HTML][HTML] Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II
HFE Gleitz, C O'Leary, RJ Holley, BW Bigger - PLoS ONE, 2017 - ncbi.nlm.nih.gov
Severe mucopolysaccharidosis type II (MPS II) is a progressive lysosomal storage disease
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II.
HFE Gleitz, C O'Leary, RJ Holley, BW Bigger - PLoS ONE, 2017 - search.ebscohost.com
Severe mucopolysaccharidosis type II (MPS II) is a progressive lysosomal storage disease
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
[引用][C] Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II
HFE Gleitz, C O'Leary, RJ Holley, BW Bigger - PLOS ONE, 2017 - cir.nii.ac.jp
Identification of age-dependent motor and neuropsychological behavioural abnormalities in
a mouse model of Mucopolysaccharidosis Type II | CiNii Research CiNii 国立情報学研究所 …
a mouse model of Mucopolysaccharidosis Type II | CiNii Research CiNii 国立情報学研究所 …
Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II.
HF Gleitz, C O'Leary, RJ Holley, BW Bigger - Plos one, 2017 - europepmc.org
Severe mucopolysaccharidosis type II (MPS II) is a progressive lysosomal storage disease
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
Identification of age-dependent motor and neuropsychological behavioural abnormalities in a mouse model of Mucopolysaccharidosis Type II
HFE Gleitz, C O'Leary, RJ Holley, BW Bigger - PLoS ONE, 2017 - go.gale.com
Severe mucopolysaccharidosis type II (MPS II) is a progressive lysosomal storage disease
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
caused by mutations in the IDS gene, leading to a deficiency in the iduronate-2-sulfatase …
