Global distribution of Fatal familial insomnia: founder or recurrent mutations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10048-008-0135-3.pdf
Reference3 articles.
1. Rodríguez-Martínez AB, Alfonso-Sánchez MA, Peña JA, Sánchez-Valle R, Zerr I, Capellari S, Calero M, Zarranz JJ, de Pancorbo MM (2008) Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation. Neurogenetics 9:109–118
2. Stacey SN, Sulem P, Johannsson OT, Helgason A, Gudmundsson J, Kostic JP, Kristjansson K, Jonsdottir T, Sigurdsson H, Hrafnkelsson J, Johannsson J, Sveinsson T, Myrdal G, Grimsson HN, Bergthorsson JT, Amundadottir LT, Gulcher JR, Thorsteinsdottir U, Kong A, Stefansson K (2006) The BARD1 Cys557Ser variant and breast cancer risk in Iceland. PLoS Med 3:1103–1113
3. Dagvadorj A, Petersen RB, Lee HS, Cervenakova L, Shatunov A, Budka H, Brown P, Gambetti P, Goldfarb LG (2002) Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy. Ann Neurol 52:355–359
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1. Fatal familial insomnia and sporadic fatal insomnia;Human Prion Diseases;2018
2. Current Infection Control Recommendations for Prion Disease; A Difficult Problem for the Deployed Personnel of the Armed Forces;Journal of Archives in Military Medicine;2017-12-02
3. Founder effect and recurrent mutational events in fatal familial insomnia;Neurogenetics;2008-06-21
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