Variant CJD in an individual heterozygous for PRNP codon 129 (Q82681101)

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17 January 2020

title

Variant CJD in an individual heterozygous for PRNP codon 129 (English)

1 reference

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17 January 2020

1 reference

1

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17 January 2020

8

John Collinge

1 reference

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17 January 2020

7

Richard Knight

1 reference

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17 January 2020

author name string

Simon Mead

2

1 reference

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17 January 2020

Harpreet Hyare

3

1 reference

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17 January 2020

Sarah Cooper

4

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17 January 2020

Ravi Jampana

5

1 reference

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17 January 2020

James Overell

6

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17 January 2020

Peter Rudge

9

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17 January 2020

language of work or name

English

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publication date

1 December 2009

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17 January 2020

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17 January 2020

volume

374

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17 January 2020

issue

9707

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17 January 2020

page(s)

2128

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Prion diseases of humans and animals: their causes and molecular basis

17 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2809%2961568-3

7 January 2021

Kuru in the 21st century--an acquired human prion disease with very long incubation periods

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2809%2961568-3

7 January 2021

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2809%2961568-3

7 January 2021

Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2809%2961568-3

7 January 2021

Human prion protein with valine 129 prevents expression of variant CJD phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2809%2961568-3

7 January 2021

10.1016/S0140-6736(09)61568-3

Identifiers

DOI

1 reference

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17 January 2020

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