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.
Abstract
摘要
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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.
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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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Alpha-synuclein expression in substantia nigra and cortex in Parkinson's disease.
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