(Q48352346)

English

Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene.

scientific article published in April 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene. (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

prion protein family

0 references

6

object named as

Lantos P

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

author name string

King A

1

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

Doey L

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

Rossor M

3

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

Mead S

4

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

Collinge J

5

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

publication date

1 April 2003

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

Neuropathology and Applied Neurobiology

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

29

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

98-105

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2990.2003.00423.X

21 January 2018

Fatal familial insomnia: clinical and pathologic heterogeneity in genetic half brothers.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2990.2003.00423.X

21 January 2018

An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2990.2003.00423.X

21 January 2018

Identifiers

10.1046/J.1365-2990.2003.00423.X

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

release_fgjfabq5drfadapyxof5fo7d54

1 reference

https://api.fatcat.wiki/v0/release/fgjfabq5drfadapyxof5fo7d54

24 November 2022

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mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/12662318

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