Parkinson's genetics: Molecular insights for the new millennium

被引:17
作者
Skipper, L [1 ]
Farrer, M [1 ]
机构
[1] Mayo Clin, Lab Familial Movement Disorders, Jacksonville, FL 32224 USA
关键词
familial parkinsonism; molecular genetics;
D O I
10.1016/S0161-813X(02)00038-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In idiopathic Parkinson's disease and familial parkinsonism, the limited number of overlapping clinical and pathological outcomes argue that a common underlying molecular pathway is perturbed. Genetic methods are a powerful approach to identify molecular components of disease. We summarize recent attempts to identify the genetic components of familial parkinsonism, without a priori assumptions about disease causation. Much effort has been expended on mapping in families with early-onset disease, in which parkinsonism appears inherited as a Mendelian trait. More recently, association methods have been employed in late-onset disease using affected sib-pairs and population isolates. These findings have been extrapolated to Parkinson's disease in the community with some success. We review the molecular synthesis now emerging from a genetic perspective. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:503 / 514
页数:12
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