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Issue Date
Title
Author(s)
1999
Prevalence of lysosomal storage disorders
Meikle, P.
;
Hopwood, J.
;
Clague, A.
;
Carey, W.
1999
Expression and characterization of wild type and mutant recombinant human sulfamidase - Implications for Sanfilippo (mucopolysaccharidosis IIIA) syndrome
Perkins, K.
;
Byers, S.
;
Yogalingam, G.
;
Weber, B.
;
Hopwood, J.
1999
Advantages of using same species enzyme for replacement therapy in a feline model of mucopolysaccharidosis type VI
Bielicki, J.
;
Crawley, A.
;
Davey, R.
;
Varnai, J.
;
Hopwood, J.
1999
Regulation of N-acetylgalactosamine 4-sulfatase expression in retrovirus-transduced feline mucopolysaccharidosis type VI muscle cells
Yogalingam, G.
;
Muller, V.
;
Hopwood, J.
;
Anson, D.
1999
Sanfilippo type B syndrome (mucopolysaccharidosis III B): allelic heterogeneity corresponds to the wide spectrum of clinical phenotypes
Weber, B.
;
Guo, X.H.
;
Kleijer, W.
;
van de Kamp, J.
;
Poorthuis, B.
;
Hopwood, J.
1999
Altered trafficking and turnover of LAMP-1 in Pompe disease-affected cells
Meikle, P.
;
Yan, M.
;
Ravenscroft, E.
;
Isaac, E.
;
Hopwood, J.
;
Brooks, D.
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Author
2
Meikle, P.
2
Weber, B.
2
Yogalingam, G.
1
Anson, D.
1
Bielicki, J.
1
Brooks, D.
1
Byers, S.
1
Carey, W.
1
Clague, A.
1
Crawley, A.
.
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Subject
3
Animals
2
Cats
2
Cell Line
2
Mucopolysaccharidosis III
2
Mucopolysaccharidosis VI
2
Mutation
2
N-Acetylgalactosamine-4-Sulfatase
2
Phenotype
2
Recombinant Proteins
1
Acetylglucosaminidase
.
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