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机译:BTNL2的截短剪接位点突变与多发性硬化的关联是HLA-DRB1 * 15的继发性因素
Cambridge Institute for Medical Research Wellcome Trust/MRC Building Addenbrooke's Hospital Cambridge CB2 2XY UK;
Division of Epidemiology School of Public Health University of California Berkeley CA 94720-7360 USA;
Department of Neurology and Human Genetics Program School of Medicine University of California San Francisco CA 94143-0435 USA;
Division of Research Kaiser Permanente Oakland CA 94612 USA and;
Department of Clinical Neurosciences University of Cambridge Addenbrooke's Hospital Hills Road Cambridge CB2 2QQ UK;
机译:BTNL2中的截短剪接位点突变与多发性硬化的关联是HLA-DRB1 * 15的继发因素。
机译:结核,麻风病和克罗恩氏病中BTNL2截短剪接位点突变的分析。
机译:结节病与BTNL2中的截短剪接位点突变有关
机译:具有内含性10 + 14剪接部位Tau基因突变模拟佩里综合征的胁迫
机译:人类遗传疾病的多种机制:COL1A2基因的剪接顺序确定。影响成骨不全症中剪接位点突变和易位破坏SNRPN基因的效应会导致Prader-Willi综合征。
机译:HLA-DRB1 * 15与多发性硬化症的关联在多代意大利家庭中得到证实
机译:错误:逆变:rarigationosis与基因Btnl2中的截断剪接位点突变有关