Reply to: SNCA variants are associated with increased risk of multiple system atrophy.
作者信息
Ross Owen A, Vilariño-Güell Carles, Wszolek Zbigniew K, Farrer Matthew J, Dickson Dennis W
出版信息
Ann Neurol. 2010 Mar;67(3):414-5. doi: 10.1002/ana.21786.
Abstract
摘要
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Reply to: SNCA variants are associated with increased risk of multiple system atrophy.回复：α-突触核蛋白（SNCA）变体与多系统萎缩风险增加有关。
Ann Neurol. 2010 Mar;67(3):414-5. doi: 10.1002/ana.21786.
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SNCA variants are associated with increased risk for multiple system atrophy.突触核蛋白α（SNCA）变体与多系统萎缩风险增加相关。
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Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.在中国人群中，α-突触核蛋白（SNCA）的基因变异与帕金森病的易感性相关，但与肌萎缩侧索硬化症或多系统萎缩无关。
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Somatic copy number gains of α-synuclein (SNCA) in Parkinson's disease and multiple system atrophy brains.帕金森病和多系统萎缩大脑中 α-突触核蛋白（SNCA）的体细胞拷贝数增加。
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MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy.微管相关蛋白tau（MAPT）H1单倍型是特发性震颤和多系统萎缩的一个风险因素。
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SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population.在中国人群中，SNCA基因的单核苷酸多态性rs11931074可能与多系统萎缩无关。
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本文引用的文献
1
SNCA variants are associated with increased risk for multiple system atrophy.突触核蛋白α（SNCA）变体与多系统萎缩风险增加相关。
Ann Neurol. 2009 May;65(5):610-4. doi: 10.1002/ana.21685.
2
alpha-Synuclein and Parkinson disease susceptibility.α-突触核蛋白与帕金森病易感性
Neurology. 2007 Oct 30;69(18):1745-50. doi: 10.1212/01.wnl.0000275524.15125.f4. Epub 2007 Sep 13.
3
Familial genes in sporadic disease: common variants of alpha-synuclein gene associate with Parkinson's disease.散发性疾病中的家族基因：α-突触核蛋白基因的常见变异与帕金森病相关。
Mech Ageing Dev. 2007 May-Jun;128(5-6):378-82. doi: 10.1016/j.mad.2007.04.002. Epub 2007 Apr 24.
4
Quantitative PCR-based screening of alpha-synuclein multiplication in multiple system atrophy.基于定量PCR的多系统萎缩中α-突触核蛋白倍增的筛查
Parkinsonism Relat Disord. 2007 Aug;13(6):340-2. doi: 10.1016/j.parkreldis.2006.12.005. Epub 2007 Feb 8.
5
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.由于α-突触核蛋白（SNCA）基因重复和三倍体导致的一个大型瑞典家系中的表型变异。
Neurology. 2007 Mar 20;68(12):916-22. doi: 10.1212/01.wnl.0000254458.17630.c5. Epub 2007 Jan 24.
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