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Association of mannose-binding lectin 2 gene polymorphisms with Guillain-Barré syndrome

Association of mannose-binding lectin 2 gene polymorphisms with Guillain-Barré syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_c8c3149c0d5f49fdb9558745fb2e7cfd

Association of mannose-binding lectin 2 gene polymorphisms with Guillain-Barré syndrome

About this item

Full title

Association of mannose-binding lectin 2 gene polymorphisms with Guillain-Barré syndrome

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2022-04, Vol.12 (1), p.5791-5791, Article 5791

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Complement activation plays a critical role in the pathogenesis of Guillain-Barré syndrome (GBS), a debilitating immune-mediated neuropathy. Mannose-binding lectin (MBL) is a complement activation factor of lectin pathway which as genetic host factor may influence the susceptibility or severity of GBS. We investigated the frequency of
MBL2
pr...

Alternative Titles

Full title

Association of mannose-binding lectin 2 gene polymorphisms with Guillain-Barré syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_c8c3149c0d5f49fdb9558745fb2e7cfd

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_c8c3149c0d5f49fdb9558745fb2e7cfd

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-022-09621-y

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