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Mucopolysaccharidosis: A broad review

Mucopolysaccharidosis: A broad review

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2a6f4faf1d2d41f7a28e363cb0f968d2

Mucopolysaccharidosis: A broad review

About this item

Full title

Mucopolysaccharidosis: A broad review

Publisher

Mumbai: Wolters Kluwer India Pvt. Ltd

Journal title

Indian journal of ophthalmology, 2022-07, Vol.70 (7), p.2249-2261

Language

English

Formats

Publication information

Publisher

Mumbai: Wolters Kluwer India Pvt. Ltd

More information

Scope and Contents

Contents

Mucopolysaccharidosis (MPS) is a group of genetic disorders with seven types and 13 subgroups which are characterized by an inherent deficiency of the enzymes responsible for the degradation of glycosaminoglycans (GAGs). Defective breakdown of GAG products leads to their widespread accumulation within the lysosomes of various organs involving the e...

Alternative Titles

Full title

Mucopolysaccharidosis: A broad review

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_2a6f4faf1d2d41f7a28e363cb0f968d2

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2a6f4faf1d2d41f7a28e363cb0f968d2

Other Identifiers

ISSN

0301-4738

E-ISSN

1998-3689

DOI

10.4103/ijo.IJO_425_22

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