Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutation-Reference-Cited by-同舟云学术

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Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutation

Published:2013-11 Issue:6 Volume:7 Page:501-510
ISSN:1933-6896
Container-title:Prion
language:en
Short-container-title:Prion

Author:

Paucar Martin,Xiang Fengqing,Moore Richard,Walker Ruth H,Winnberg Elisabeth,Svenningsson Per

Publisher

Informa UK Limited

Subject

Infectious Diseases,Cell Biology,Cellular and Molecular Neuroscience,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.4161/pri.27260

Reference36 articles.

1. Prion disease genetics

2. The genetics of prion diseases

3. Clinical Characterization of a Kindred With a Novel 12-Octapeptide Repeat Insertion in the Prion Protein Gene

4. Genetics of Prion Disease

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1. Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP);Journal of Neurology;2023-09-09

2. Four Octapeptide Repeat Insertion (4-OPRI) in PRNP Causing Huntington Disease Phenocopy;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;2023-08-24

3. Diagnostic Uncertainties: Chorea;Seminars in Neurology;2023-02

4. Human prion diseases and the prion protein – what is the current state of knowledge?;Translational Neuroscience;2023-01-01

5. The importance of ongoing international surveillance for Creutzfeldt–Jakob disease;Nature Reviews Neurology;2021-05-10

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