(Q40654350)

22 September 2017

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title

Molecular genetic studies of Creutzfeldt-Jakob disease (English)

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22 September 2017

L G Goldfarb

1

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22 September 2017

P Brown

series ordinal

2

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22 September 2017

L Cervenakova

series ordinal

3

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22 September 2017

D C Gajdusek

series ordinal

4

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22 September 2017

publication date

1 April 1994

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22 September 2017

published in

Molecular Neurobiology

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22 September 2017

volume

8

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22 September 2017

issue

2-3

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22 September 2017

page(s)

89-97

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Single nucleotide primer extension to detect genetic diseases: experimental application to hemophilia B (factor IX) and cystic fibrosis genes

22 September 2017

cites work

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12 December 2020

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

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12 December 2020

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

1 reference

12 December 2020

Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils

1 reference

12 December 2020

Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20.

1 reference

12 December 2020

A dementing illness associated with a novel insertion in the prion protein gene

1 reference

12 December 2020

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

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12 December 2020

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease

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12 December 2020

Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

1 reference

12 December 2020

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features

1 reference

12 December 2020

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies

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12 December 2020

Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families

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12 December 2020

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

1 reference

12 December 2020

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

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12 December 2020

The molecular genetics of familial Creutzfeldt-Jakob disease in France

1 reference

12 December 2020

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease

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12 December 2020

Molecular biology of prion diseases

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12 December 2020

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

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12 December 2020

Identifiers

DOI

10.1007/BF02780658

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Dimensions Publication ID

22 September 2017

1008008694

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