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Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1321793017

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

Publication information

Publisher

London: Nature Publishing Group UK

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Scope and Contents

Contents

Algorithms designed to identify canonical yeast prions predict that around 250 human proteins, including several RNA-binding proteins associated with neurodegenerative disease, harbour a distinctive prion-like domain (PrLD) enriched in uncharged polar amino acids and glycine. PrLDs in RNA-binding proteins are essential for the assembly of ribonucle...

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Full title

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

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Record Identifier

TN_cdi_proquest_miscellaneous_1321793017

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1321793017

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ISSN

0028-0836,1476-4687

E-ISSN

1476-4687

DOI

10.1038/nature11922

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