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The patient journey of patients with Fabry disease, Gaucher disease and Mucopolysaccharidosis type I...

The patient journey of patients with Fabry disease, Gaucher disease and Mucopolysaccharidosis type I...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2474468988

The patient journey of patients with Fabry disease, Gaucher disease and Mucopolysaccharidosis type II: A German-wide telephone survey

About this item

Full title

The patient journey of patients with Fabry disease, Gaucher disease and Mucopolysaccharidosis type II: A German-wide telephone survey

Publisher

United States: Public Library of Science

Journal title

PloS one, 2020-12, Vol.15 (12), p.e0244279-e0244279

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Lysosomal Storage Diseases (LSD) are rare and multisytemic diseases which are caused by lysosomal enzyme deficiencies leading into accumulation of waste products due to an interruption in the decomposition process. Due to the low prevalence and therefore limited disease awareness as well as the fact that LSD patients present with unspecific symptom...

Alternative Titles

Full title

The patient journey of patients with Fabry disease, Gaucher disease and Mucopolysaccharidosis type II: A German-wide telephone survey

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_2474468988

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2474468988

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0244279

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