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Prions, prion-like prionoids, and neurodegenerative disordersVacancy

Prions, prion-like prionoids, and neurodegenerative disordersVacancy

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3a24540ac90045eaa46ef359fdc43c96

Prions, prion-like prionoids, and neurodegenerative disordersVacancy

About this item

Full title

Prions, prion-like prionoids, and neurodegenerative disordersVacancy

Author / Creator

Publisher

Mumbai: Wolters Kluwer - Medknow Publications

Journal title

Annals of the Indian Academy of Neurology, 2016-04, Vol.19 (2), p.169-174

Language

English

Formats

Publication information

Publisher

Mumbai: Wolters Kluwer - Medknow Publications

More information

Scope and Contents

Contents

Prion diseases or transmissible spongiform encephalopathies are fatal neurodegenerative diseases characterized by the aggregation and deposition of the misfolded prion protein in the brain. α-synuclein (α-syn)-associated multiple system atrophy has been recently shown to be caused by a bona fide α-syn prion strain. Several other misfolded native pr...

Alternative Titles

Full title

Prions, prion-like prionoids, and neurodegenerative disordersVacancy

Authors, Artists and Contributors

Author / Creator

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_3a24540ac90045eaa46ef359fdc43c96

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3a24540ac90045eaa46ef359fdc43c96

Other Identifiers

ISSN

0972-2327

E-ISSN

1998-3549

DOI

10.4103/0972-2327.179979

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