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机译:具有新型PINK1突变的帕金森家族的临床和分子表征
Hertie-Institute for Clinical Brain Research Dept. for Neurodegenerative Diseases University of Tuebingen Hoppe-Seyler-Str. 3 72076 Tuebingen Germany;
Metabolic Disease Center Hospital Munich-Schwabing Munich Germany;
Dept. of Neuroradiology Radiological Clinic of the University of Tuebingen Germany;
Hertie-Institute for Clinical Brain Research Dept. for Neurodegenerative Diseases University of Tuebingen Hoppe-Seyler-Str. 3 72076 Tuebingen Germany;
Institute of Human Genetics GSF National Research Center Munich-Neuherberg Germany;
Institute of Human Genetics GSF National Research Center Munich-Neuherberg Germany;
Dept. of Neurosurgery University of Tuebingen Germany;
Dept. of Neuroradiology Radiological Clinic of the University of Tuebingen Germany;
Dept. of Neuroradiology Radiological Clinic of the University of Tuebingen Germany;
Hertie-Institute for Clinical Brain Research Dept. for Neurodegenerative Diseases University of Tuebingen Hoppe-Seyler-Str. 3 72076 Tuebingen Germany;
Dept. of Neurology Klinikum Grosshadern Ludwig-Maximilians-University Munich Germany;
Hertie-Institute for Clinical Brain Research Dept. for Neurodegenerative Diseases University of Tuebingen Hoppe-Seyler-Str. 3 72076 Tuebingen Germany;
parkinson; PINK1; genetics; MR spectroscopy;
机译:具有新型PINK1突变的帕金森家族的临床和分子表征。
机译:德国家庭中PINK1突变的体感处理:其在帕金森氏病中的潜在作用。
机译:由PINK1突变引起的迟发性散发性帕金森氏病:临床和功能研究。
机译:GHRH受体突变的分子与临床方面
机译:功能性蛋氨酸合酶缺乏症的分子遗传学和表征:突变分析和基因克隆。
机译:50个常染色体隐性帕金森病家族揭示已知和新型基因突变的临床和分子遗传学研究
机译:帕金森病的大型德国家庭纯合和杂合粉红色突变的临床谱