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机译:在汉族人口中没有帕金森病或肌营养的侧面硬化,缺乏ALA58VAL(RS17571)CTSD基因变异的关联
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Kunming Med Univ Affiliated Hosp 1 Dept Geriatr Neurol Kunming 650032 Yunnan Peoples R China;
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Sichuan Univ West China Hosp Dept Neurol 37 Guo Xue Xiang Chengdu 610041 Sichuan Peoples R;
Parkinson's disease; Amyotrophic lateral sclerosis; Alzheimer's disease; CTSD gene; rs17571;
机译:在汉族人口中没有帕金森病或肌营养的侧面硬化,缺乏ALA58VAL(RS17571)CTSD基因变异的关联
机译:缺乏证据表明汉族人群中COQ2的V393A变异与肌萎缩性侧索硬化之间存在关联
机译:ZNF512B中功能性SNP rs2275294与肌萎缩性侧索硬化症和帕金森氏病风险的相关性
机译:PERFORM:监测和管理慢性神经退行性疾病的平台:帕金森氏症和肌萎缩性侧索硬化症
机译:生殖史和药物是肌萎缩性侧索硬化症和帕金森氏病的危险因素。
机译:SNCA的遗传变异与帕金森氏病的易感性相关但与中国人群的肌萎缩性侧索硬化或多系统萎缩无关
机译:sNCa的遗传变异与帕金森病的易感性相关,但与中国人群的肌萎缩性侧索硬化或多系统萎缩无关。