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Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease.法国家族性和散发性帕金森病患者α-突触核蛋白基因中不存在G209A突变。
J Neurol Neurosurg Psychiatry. 1998 Dec;65(6):948-9. doi: 10.1136/jnnp.65.6.948.
2
No mutation of G209A in the alpha-synuclein gene in sporadic Parkinson's disease among Taiwan Chinese.台湾华裔散发性帕金森病患者中α-突触核蛋白基因未发生G209A突变。
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The role of the alpha-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom.α-突触核蛋白基因突变在英国散发性帕金森病患者中的作用。
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Absence of G209A and G88C mutations in the alpha-synuclein gene of Parkinson's disease in a Chinese population.中国人群帕金森病α-突触核蛋白基因中不存在G209A和G88C突变。
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A case of late onset sporadic Parkinson's disease with an A53T mutation in alpha-synuclein.一例伴有α-突触核蛋白A53T突变的迟发性散发性帕金森病。
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The G209A mutation in the alpha-synuclein gene is not detected in familial cases of Parkinson disease in non-Greek and/or Italian populations.在非希腊和/或意大利人群的帕金森病家族病例中未检测到α-突触核蛋白基因的G209A突变。
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Failure to find the alpha-synuclein gene missense mutation (G209A) in 100 patients with younger onset Parkinson's disease.在100例早发型帕金森病患者中未发现α-突触核蛋白基因错义突变（G209A）。
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Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's disease.帕金森病中α-突触核蛋白的突变、序列分析及关联研究。
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引用本文的文献

1
The heterozygous A53T mutation in the alpha-synuclein gene in a Chinese Han patient with Parkinson disease: case report and literature review.一名中国汉族帕金森病患者α-突触核蛋白基因杂合A53T突变：病例报告及文献复习
J Neurol. 2016 Oct;263(10):1984-92. doi: 10.1007/s00415-016-8213-1. Epub 2016 Jul 8.
2
Clinical phenotype in patients with alpha-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease.与散发性帕金森病患者相比，居住在希腊的α-突触核蛋白帕金森病患者的临床表型。
J Neurol Neurosurg Psychiatry. 2001 May;70(5):662-5. doi: 10.1136/jnnp.70.5.662.

Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease.

作者信息

Lucotte G, Mercier G, Turpin J C

出版信息

J Neurol Neurosurg Psychiatry. 1998 Dec;65(6):948-9. doi: 10.1136/jnnp.65.6.948.

DOI:10.1136/jnnp.65.6.948
PMID:9854985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2170420/
Abstract
摘要