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Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases

Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2648065189

Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases

About this item

Full title

Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases

Publisher

London: BMJ Publishing Group Ltd

Journal title

Journal of neurology, neurosurgery and psychiatry, 2022-07, Vol.93 (7), p.779-784

Language

English

Formats

Publication information

Publisher

London: BMJ Publishing Group Ltd

More information

Scope and Contents

Contents

BackgroundNo studies have assessed the independent association of methionine homozygosity at codon 129 with the susceptibility to prion diseases, controlling for the effects of the codon 219 polymorphisms and other potential confounders, using a large-scale population-based dataset.MethodsWe conducted a case-control study using a Japanese nationwid...

Alternative Titles

Full title

Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2648065189

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2648065189

Other Identifiers

ISSN

0022-3050

E-ISSN

1468-330X

DOI

10.1136/jnnp-2021-328720

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