机译:晚期遗传性感和自主神经病变扩大了MFN2 MFN2-相关疾病的表型谱
Department of NeurologyPeking University First HospitalBeijing China;
Department of NeurologyPeking University First HospitalBeijing China;
Department of NeurologyPeking University First HospitalBeijing China;
Department of NeurologyPeking University First HospitalBeijing China;
Department of NeurologyPeking University First HospitalBeijing China;
Department of NeurologyPeking University First HospitalBeijing China;
MFN2; Charcot‐Marie‐Tooth disease; hereditary sensory and autonomic neuropathy; sural nerve biopsy;
机译:晚期遗传性感和自主神经病变扩大了MFN2 MFN2-相关疾病的表型谱
机译:MFN2基因突变的频谱和频率及其表型表达在捷克遗传性运动和感觉神经病II型患者中
机译:迟发性遗传感觉和自主神经病伴Y163X ion病毒突变引起的认知障碍
机译:俄罗斯人群遗传疾病基因的突变谱
机译:Leber遗传性视神经病变和Stargardt病的综述:遗传咨询员在应对这两种疾病时的舒适度
机译:迟发性遗传感觉和自主神经病伴Y163X sensor病毒突变引起的认知障碍
机译:迟发性遗传感觉和自主神经病变伴有Y163X pr病毒突变引起的认知障碍。