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Genome wide association study of clinical duration and age at onset of sporadic CJD

Genome wide association study of clinical duration and age at onset of sporadic CJD

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_3085092325

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Human prion diseases are rare, transmissible and often rapidly progressive dementias. The most common type, sporadic Creutzfeldt-Jakob disease (sCJD), is highly variable in clinical duration and age at onset. Genetic determinants of late onset or slower progression might suggest new targets for research and therapeutics. We assembled and array geno...

Alternative Titles

Full title

Genome wide association study of clinical duration and age at onset of sporadic CJD

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_3085092325

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_3085092325

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0304528

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