Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain.

Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain.
复制标题

DOI:
10.1007/s10048-009-0187-z
复制
发表时间:
2009-10
期刊:
影响因子:
2.2
通讯作者:
Zabetian, Cyrus P.
Zabetian, Cyrus P.
中科院分区:
医学3区
文献类型:
--
作者:
Mata, Ignacio F.;Hutter, Carolyn M.;Gonzalez-Fernandez, Maria C.;de Pancorbo, Marian M.;Lezcano, Elena;Huerta, Cecilia;Blazquez, Marta;Ribacoba, Renee;Guisasola, Luis M.;Salvador, Carlos;Gomez-Esteban, Juan C.;Zarranz, Juan J.;Infante, Jon;Jankovic, Joseph;Deng, Hao;Edwards, Karen L.;Alvarez, Victoria;Zabetian, Cyrus P.

文献摘要

参考文献

被引文献

相似文献

Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene together represent the most common genetic determinant of Parkinson's disease (PD) identified to date. The vast majority of patients with LRRK2-related PD reported in the literature carry one of three pathogenic substitutions: G2019S, R1441C, or R1441G. While G2019S and R1441C are geographically widespread, R1441G is most prevalent in the Basque Country and is rare outside of Northern Spain. We sought to better understand the processes that have shaped the current distribution of R1441G. We performed a haplotype analysis of 29 unrelated PD patients heterozygous for R1441G and 85 wild-type controls using 20 markers that spanned 15.1 Mb across the LRRK2 region. Nine of the patients were of Basque origin and 20 were non-Basques. We inferred haplotypes using a Bayesian approach and utilized a maximum-likelihood method to estimate the age of the most recent common ancestor. Significant but incomplete allele sharing was observed over a distance of 6.0 Mb and a single, rare ten-marker haplotype 5.8 Mb in length was seen in all mutation carriers. We estimate that the most recent common ancestor lived 1,350 (95% CI, 1,020–1,740) years ago in approximately the seventh century. We hypothesize that R1441G originated in the Basque population and that dispersion of the mutation then occurred through short-range gene flow that was largely limited to nearby regions in Spain.
DOI: 10.1136/jmg.2005.035568
发表时间: 2005-11-01
影响因子: 4
作者:
Goldwurm, S;Di Fonzo, A;Bonifati, V
通讯作者: Bonifati, V
DOI: 10.1001/archneur.63.3.377
发表时间: 2006-03-01
影响因子: --
作者:
Gaig, C;Ezquerra, M;Tolosa, E
通讯作者: Tolosa, E
DOI: 10.1002/ajpa.20188
发表时间: 2005-10-01
影响因子: 2.8
作者:
Fenner, JN
通讯作者: Fenner, JN
DOI: 10.1086/302617
发表时间: 1999-11-01
影响因子: 9.8
作者:
Hurles, ME;Veitia, R;Jobling, MA
通讯作者: Jobling, MA
DOI: 10.1093/brain/awh666
发表时间: 2005-12-01
期刊: BRAIN
影响因子: 14.5
作者:
Berg, D;Schweitzer, KJ;Gasser, T
通讯作者: Gasser, T