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机译:FMR1突变前等位基因男性携带者的成纤维细胞表型
Department of Biochemistry and Molecular Medicine and;
Department of Biochemistry and Molecular Medicine and;
CBG-Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands,;
Department of Biochemistry and Molecular Medicine and|M.I.N.D. Institute,;
Department of Biochemistry and Molecular Medicine and;
Departments of Pediatrics, Neurological Sciences, and Biochemistry,;
Departments of Neurological Sciences and Pharmacology and;
Department of Pediatrics, Rush University Medical Center, Chicago, IL, USA;
Department of Pediatrics, Rush University Medical Center, Chicago, IL, USA;
Division of Biostatistics, Department of Public Health Sciences, School of Medicine, University of California, Davis, CA, USA,;
Division of Biostatistics, Department of Public Health Sciences, School of Medicine, University of California, Davis, CA, USA,;
Department of Biochemistry and Molecular Medicine and;
Department of Biochemistry and Molecular Medicine and;
Department of Pathology and;
CBG-Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands,;
M.I.N.D. Institute,|Department of Pediatrics, University of California, Davis, Health System, Sacramento, CA, USA,;
机译:FMR1突变前等位基因男性携带者的成纤维细胞表型。
机译:一般人群中有10572名男性中的FMR1等位基因突变和中等大小:AGG中断的缺失是易碎X综合征等位基因产生的晚期事件。
机译:FMR1基因易碎的X相关震颤/共济失调综合征对正常和突变前等位基因男性运动纤维束的影响
机译:使用源定位对动态摇摆任务中FMR1突变载体的神经活动进行量化*
机译:从表型到蛋白质折叠:伴侣蛋白和伴侣蛋白等位基因之间等位基因依赖性遗传相互作用的表征。
机译:FMR1突变前等位基因男性携带者的成纤维细胞表型
机译:FMR1突变前等位基因男性携带者的成纤维细胞表型