机译:墨西哥人口1型突变突变的起源及美洲印第安人祖先对CTG重复等位基因分布的影响
Laboratory of Genomic Medicine Department of Genetics National Rehabilitation Institute (INR);
Laboratory of Genomic Medicine Department of Genetics National Rehabilitation Institute (INR);
Department of Toxicology CINVESTAV-IPN;
Laboratory of Immunogenomics and Metabolic Diseases National Genomic Medicine Institute (INMEGEN);
Laboratory of Immunogenomics and Metabolic Diseases National Genomic Medicine Institute (INMEGEN);
Laboratory of Genomic Medicine Department of Genetics National Rehabilitation Institute (INR);
Department of Toxicology CINVESTAV-IPN;
Laboratory of Genomic Medicine Department of Genetics National Rehabilitation Institute (INR);
Laboratory of Sinovial Liquid INR;
Laboratory of Diagnostic Molecular Biology (BIMODI);
Laboratory of Diagnostic Molecular Biology (BIMODI);
Laboratory of Genomic Medicine Department of Genetics National Rehabilitation Institute (INR);
Department of Genetics and Molecular Biology Center of Research and Advanced Studies-National;
Laboratory of Genomic Medicine Department of Genetics National Rehabilitation Institute (INR);
Myotonic dystrophy type 1; CTG repeats; Amerindian population; Mexican mestizo population; Haplotype; Polymorphism;
机译:墨西哥人口1型突变突变的起源及美洲印第安人祖先对CTG重复等位基因分布的影响
机译:在CTG扩展范围内,CCG和GGC重复出现变异,大大改变了突变动力学,并可能导致某些强直性营养不良1型患者的异常症状
机译:在特定组织中用“非CTG重复”插入物代替1型强直性肌营养不良性CTG重复。
机译:1型强直性营养不良中的DNA复制和与疾病相关的三核苷酸重复不稳定性。
机译:用特定组织中的非CTG重复插入替换肌肌营养不良1型CTG重复
机译:用“非CTG重复”在特定组织中插入替换肌肌营养不良1型CTG重复