Ancestral origins of the prion protein gene D178N mutation in the Basque Country-Reference-Cited by-同舟云学术

Ancestral origins of the prion protein gene D178N mutation in the Basque Country

Published:2005-04-02 Issue:1 Volume:117 Page:61-69
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Rodríguez-Martínez Ana B.,Barreau Christian,Coupry Isabelle,Yagüe Jordi,Sánchez-Valle Raquel,Galdós-Alcelay Luis,Ibáñez Agustín,Digón Antón,Fernández-Manchola Ignacio,Goizet Cyril,Castro Azucena,Cuevas Nerea,Alvarez-Alvarez Maite,de Pancorbo Marian M.,Arveiler Benoît,Zarranz Juan J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-005-1277-0.pdf

Reference38 articles.

1. Alonso S, Castro A, Fernández I, Gomez de Cedron M, Garcia-Orad A, Meyer E, Martinez De Pancorbo M (1995) Population study of 3 STR loci in de Basque country (northern Spain). Int J Leg Med 107:239–245

2. Brown DR (2002) Molecular advances in understanding inherited prion diseases. Mol Neurobiol 25:287–301

3. Brown P, Cervenakova L, Goldfarb LG, McCombie WR, Rubenstein R, Will RG, Pocchiari M, Martinez-Lage JF, Scalici C, Masullo C, et al (1994) Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine. Neurology 44:291–293

4. Collins A, Lanjou C, Morton NE (1999) Genetic epidemiology of single-nucleotide polymorphisms. Proc Natl Acad Sci USA 96:15173–15177

5. Dagvadorj A, Petersen RB, Lee HS, Cervenakova L, Shatunov A, Budka H, Brown P, Gambetti P, Goldfarb LG (2002) Spontaneous mutation in the prion protein gene causing transmissible spongiform encephalopathies. Ann Neurol 52:355–359

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Creutzfeldt–Jakob Disease and Fatal Familial Insomnia: Demographics and In-Hospital Mortality in Spain;Journal of Clinical Medicine;2024-07-27

2. Human prion disease surveillance in Spain, 1993-2018: an overview;Prion;2021-01-01

3. Neurogenetic Disorders in the Basque Population;Annals of Human Genetics;2014-12-01

4. Genetic Creutzfeldt–Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis;Acta Neuropathologica;2010-10-27

5. Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2010-05-24