Genetic analysis of the ATP1B4 gene in Chinese Han patients with Parkinson’s disease

Genetic analysis of the ATP1B4 gene in Chinese Han patients with Parkinson’s disease
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中国汉族帕金森病患者ATP1B4基因遗传分析

DOI:
10.1007/s11033-014-3084-y
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发表时间:
2014-01
影响因子:
2.8
通讯作者:
Deng H
Deng H
中科院分区:
生物学4区
文献类型:
--
作者:
Deng X;Yuan Y;Zhao Y;Deng H

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帕金森病(Parkinson's disease,PD)是第二常见的神经退行性疾病,临床上以运动迟缓、静止性震颤、强直和姿势不稳为特征。ATP酶13 A2基因的突变被发现是Kufor-Rakeb synn的原因。
Parkinson’s disease (PD) is the second most common neurodegenerative disease characterized clinically by bradykinesia, resting tremor, rigidity and postural instability. Mutations in the ATPase 13A2 gene were found to be the causes for the Kufor-Rakeb syn
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