Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease. (Q46188775)

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1 November 2019

title

Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease (English)

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1 November 2019

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Sophie Mouillet-Richard

1

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1 November 2019

author name string

C Teil

2

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1 November 2019

M Lenne

3

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1 November 2019

S Hugon

4

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1 November 2019

O Taleb

5

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1 November 2019

J L Laplanche

6

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1 November 2019

publication date

1 October 1999

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Journal of the Neurological Sciences

1 November 2019

number of pages

4

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based on heuristic

inferred from page(s)

published in

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1 November 2019

volume

168

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1 November 2019

issue

2

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1 November 2019

page(s)

141-144

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Novel proteinaceous infectious particles cause scrapie

1 November 2019

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7 January 2021

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A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease

7 January 2021

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A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

7 January 2021

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A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210

7 January 2021

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Panencephalitic Creutzfeldt-Jakob disease in a Chinese family. Unusual presentation with PrP codon 210 mutation and identification by PCR-SSCP.

7 January 2021

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14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

7 January 2021

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Double-gradient DGGE for optimized detection of DNA point mutations

7 January 2021

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Deletion in prion protein gene in a Moroccan family

7 January 2021

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Deletions in the prion protein gene are not associated with CJD.

7 January 2021

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Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin

7 January 2021

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New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests

7 January 2021

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Aminoacid polymorphism in human prion protein and age at death in inherited prion disease

7 January 2021

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The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutation

7 January 2021

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7 January 2021

Identifiers

DOI

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1 November 2019

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