...
机译:Charcot-Marie-Tooth 1A型疾病基因PMP22上游的远端增强子
1Program in Cellular and Molecular Biology, 2Waisman Center, 3Department of Statistics, 4Department of Biostatistics and Medical Informatics and 5Department of Comparative Biosciences, Waisman Center, University of Wisconsin, Madison, WI 53705, USA, 6Department of Human Genetics, 7Department of Neurology, University of Michigan Medical School, Ann Arbor, MI 48109, USA;
机译:Charcot-Marie-Tooth 1A型疾病PMP22上游的远端增强子
机译:由PMP22基因中新的Ser112Arg突变引起的Charcot-Marie-Tooth 1A型疾病,与缓慢进行性听力障碍共存
机译:PMP22基因中的一种新型点突变与伴有感音神经性耳聋的Charcot-Marie-Tooth疾病1A型家族病例有关。
机译:炭疽病1A型的治疗基因组编辑
机译:糖基-tRNA合成酶突变导致2D型Charcot-Marie-Tooth病和V型远端脊髓性肌萎缩症:人类周围神经病的潜在新型疾病机制。
机译:Charcot-Marie-Tooth 1A型疾病基因PMP22上游的远端增强子
机译:Charcot-Marie-tooth型1A疾病基因PMP22上游的远端增强剂