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Mucopolysaccharide diseases: A complex interplay between neuroinflammation, microglial activation an...

Mucopolysaccharide diseases: A complex interplay between neuroinflammation, microglial activation an...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1492621931

Mucopolysaccharide diseases: A complex interplay between neuroinflammation, microglial activation and adaptive immunity

About this item

Full title

Mucopolysaccharide diseases: A complex interplay between neuroinflammation, microglial activation and adaptive immunity

Publisher

Dordrecht: Springer Netherlands

Journal title

Journal of inherited metabolic disease, 2014-01, Vol.37 (1), p.1-12

Language

English

Formats

Publication information

Publisher

Dordrecht: Springer Netherlands

More information

Scope and Contents

Contents

Mucopolysaccharide (MPS) diseases are lysosomal storage disorders (LSDs) caused by deficiencies in enzymes required for glycosaminoglycan (GAG) catabolism. Mucopolysaccharidosis I (MPS I), MPS IIIA, MPS IIIB and MPS VII are deficient in the enzymes α–L-Iduronidase, Heparan-N-Sulphatase, N-Acetylglucosaminidase and Beta-Glucuronidase, respectively....

Alternative Titles

Full title

Mucopolysaccharide diseases: A complex interplay between neuroinflammation, microglial activation and adaptive immunity

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1492621931

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1492621931

Other Identifiers

ISSN

0141-8955

E-ISSN

1573-2665

DOI

10.1007/s10545-013-9613-3

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