Molecular genetic studies of Creutzfeldt-Jakob disease (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

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3

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22 September 2017

D C Gajdusek

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4

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22 September 2017

1 April 1994

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22 September 2017

Molecular Neurobiology

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22 September 2017

8

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22 September 2017

2-3

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22 September 2017

89-97

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https://scigraph.springernature.com/pub.10.1007/bf02780658

22 September 2017

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cites work

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

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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

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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

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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.

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12 December 2020

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

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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

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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

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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

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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

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