Significant linkage of Parkinson disease to chromosome 2q36-37

被引:105
|
作者
Pankratz, N
Nichols, WC
Uniacke, SK
Halter, C
Rudolph, A
Shults, C
Conneally, PM
Foroud, T
机构
[1] Indiana Univ, Med Ctr, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[2] Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USA
[3] Univ Rochester, Dept Neurol, Rochester, NY USA
[4] Univ Calif San Diego, Dept Neurosci, San Diego, CA 92103 USA
[5] VA San Diego Healthcare Syst, San Diego, CA USA
关键词
D O I
10.1086/374383
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Parkinson disease (PD) is the second most common neurodegenerative disorder, surpassed in frequency only by Alzheimer disease. Elsewhere we have reported linkage to chromosome 2q in a sample of sibling pairs with PD. We have now expanded our sample to include 150 families meeting our strictest diagnostic definition of verified PD. To further delineate the chromosome 2q linkage, we have performed analyses using only those pedigrees with the strongest family history of PD. Linkage analyses in this subset of 65 pedigrees generated a LOD score of 5.1, which was obtained using an autosomal dominant model of disease transmission. This result strongly suggests that variation in a gene on chromosome 2q36-37 contributes to PD susceptibility.
引用
收藏
页码:1053 / 1057
页数:5
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