Age at Death of Creutzfeldt-Jakob Disease in Subsequent Family Generation Carrying the E200K Mutation of the Prion Protein Gene-Reference-Cited by-同舟云学术

Age at Death of Creutzfeldt-Jakob Disease in Subsequent Family Generation Carrying the E200K Mutation of the Prion Protein Gene

Published:2013-04-02 Issue:4 Volume:8 Page:e60376
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Pocchiari Maurizio,Poleggi Anna,Puopolo Maria,D’Alessandro Marco,Tiple Dorina,Ladogana Anna

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference32 articles.

1. Genetic prion disease: the EUROCJD experience;GG Kovacs;Human Genet,2005

2. Prion disease genetics;S Mead;Eur J Human Genet,2006

3. Kong Q, Kong Q, Surewicz WK, Petersen RB, Zou W, et al.. (2004) Inherited prion diseases. In Prusiner SB, editor. Prion Biology and Diseases. Cold Spring Harbor: Cold Spring Harbor Laboratory Press. 673–775.

4. Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia;LG Goldfarb;Lancet,1990

5. Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin;LG Goldfarb;Lancet,1990

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2. Huntington’s disease: lessons from prion disorders;Journal of Neurology;2021-02-24

3. Pseudo‐anticipation in Creutzfeldt–Jakob disease is due to a rhomboid‐shaped artifact;European Journal of Neurology;2020-02-03

4. Genetic Factors in Mammalian Prion Diseases;Annual Review of Genetics;2019-12-03

5. Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the CYP4X1 gene;Journal of Neurology, Neurosurgery & Psychiatry;2018-07-21