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Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

机译：在芬兰和希腊患者中缺乏证据表明它与FGF20 和帕金森病之间存在遗传关联

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Hadjigeorgiou George M; Papadimitriou Alexandros; Peuralinna Terhi; Dardiotis Euthimios; Hellström Olli; Gourbali Vanesa; Eerola Johanna; Xiromerisiou Georgia; Clarimon Jordi; Tienari Pentti J; Singleton Andrew B;
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1. Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients [J] . Jordi Clarimon, Georgia Xiromerisiou, Johanna Eerola, BMC Neurology . 2005,第1期

机译：芬兰和希腊患者缺乏FGF20与帕金森氏病之间遗传关联的证据
2. Genetic analysis of FGF20 in Chinese patients with Parkinson’s disease [J] . Xiao-Yi Sun, Ling Wang, Lan Cheng, Neurological sciences . 2017,第5期

机译：中国帕金森病患者FGF20的遗传分析
3. Lack of Association Between CX3CR1 V249I and T280M Polymorphisms and Risk of Parkinson's Disease in a Greek Population [J] . Kallirhoe Kalinderi, Sevasti Bostantjopoulou, Zoe Katsarou, Genetic testing and molecular biomarkers . 2012,第8期

机译：CX3CR1 V249I和T280M多态性之间缺乏关联和帕金森氏病在希腊人群中的风险。
4. Connectome Pathways in Parkinson's Disease Patients with Deep Brain Stimulators Connectome Pathways in Parkinson's Disease Patients with DBS [C] . Giorgio Bonmassar, Nikos Makris International Conference on Advanced Cognitive Technologies and Applications . 2015

机译：Connectome途径在帕金森病患者深脑刺激患者帕金森病患者DBS的疾病患者
5. Patients' opinions on genetic counseling on the increased risk of Parkinson's disease among Gaucher disease carriers [D] . Mulhern, Maureen 2015

机译：患者对高彻病携带者中帕金森氏病风险增加的遗传咨询意见
6. Lack of evidence for a genetic association between FGF20 and Parkinsons disease in Finnish and Greek patients [O] . Jordi Clarimon, Georgia Xiromerisiou, Johanna Eerola, 2005

机译：芬兰和希腊患者缺乏FGF20与帕金森氏病之间遗传关联的证据
7. Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients [O] . Jordi Clarimon, Georgia Xiromerisiou, Johanna Eerola, 2005

机译：芬兰和希腊患者缺乏FGF20与帕金森氏病之间遗传关联的证据

Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

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