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机译:患有严重早期发作性 - 玛丽牙疾病2A型患者的十五年纵向随访
Department of NeurologyJohns Hopkins University School of MedicineJohn G. Rangos Building 855;
Department of NeurologyJohns Hopkins University School of MedicineJohn G. Rangos Building 855;
Department of NeurologyJohns Hopkins University School of MedicineJohn G. Rangos Building 855;
Department of NeurologyJohns Hopkins University School of MedicineJohn G. Rangos Building 855;
axonal neuropathy; Charcot‐Marie‐Tooth disease; CMT2; CMT2A; inherited neuropathy; mitofusin 2;
机译:患有严重早期发作性 - 玛丽牙疾病2A型患者的十五年纵向随访
机译:与新发性Charcot-Marie-Tooth病2A型神经病相关的MFN2的两个从头突变
机译:PXT3003在Charcot-Marie-Tooth疾病患者中PXT3003的疗效和安全性1A:Pleo-Charcot-Marie-Toother的结果:国际关键阶段III试验
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:夏科特–玛丽–牙病1A型重复并严重下肢近端肌肉轻瘫:一项长期随访研究
机译:2型Charcot-Marie-Tooth病的病程-一项为期5年的随访研究