Article
VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China.
Neurobiology of aging - 1 Jun 2013
Chen YongPing, Chen Ke, Song Wei, Chen XuePing, Cao Bei, Huang Rui, Zhao Bi, Guo XiaoYan, Burgunder JeanMarc, Li JianPeng, Shang Hui-Fang
Abstract excerpt
The Asp620Asn mutation in the vacuolar protein sorting protein 35 (VPS35) gene and the Arg1205His mutation in the eukaryotic translation initiation factor 4 gamma 1 (EIF4G1) gene were identified in autosomal dominant late-onset familial and sporadic Parkinson disease (PD) patients in a Caucasian population. However, the frequencies of these 2 mutations among Chinese PD patients are unknown. We examined these...
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