机译:具有发育不全的肾上腺肺病患中的新型ABCD1基因突变和胼calloSum的患者
Peking Univ Dept Neurol Peoples Hosp 11 Xizhimen South Ave Beijing 100044 Peoples R China;
Univ Mississippi Dept Hlth Exercise Sci &
Recreat Management Oxford MS USA;
Nanchang Univ Affiliated Hosp 1 Dept Neurol Nanchang Jiangxi Peoples R China;
Peking Univ Dept Neurol Peoples Hosp 11 Xizhimen South Ave Beijing 100044 Peoples R China;
Peking Univ Dept Neurol Peoples Hosp 11 Xizhimen South Ave Beijing 100044 Peoples R China;
Peking Univ Dept Neurol Peoples Hosp 11 Xizhimen South Ave Beijing 100044 Peoples R China;
Peking Univ Dept Neurol Peoples Hosp 11 Xizhimen South Ave Beijing 100044 Peoples R China;
Peking Univ Dept Neurol Peoples Hosp 11 Xizhimen South Ave Beijing 100044 Peoples R China;
Nanchang Univ Affiliated Hosp 1 Dept Neurol Nanchang Jiangxi Peoples R China;
Peking Univ Dept Neurol Peoples Hosp 11 Xizhimen South Ave Beijing 100044 Peoples R China;
Adrenomyeloneuropathy; Adrenoleukodystrophy; Corpus callosum; hypoplasia and agenesis; Spastic paraplegia; Alopecia;
机译:具有发育不全的肾上腺肺病患中的新型ABCD1基因突变和胼calloSum的患者
机译:由于编码线粒体柠檬酸盐转运蛋白的SLC25A1中的突变,导致call体发育不全和视神经发育不全。
机译:由TUBA1A突变引起的明显脑室扩张、,体发育不全和小脑发育不全的小脑
机译:通过磁共振图像比较Call体退化
机译:Call体再生中动画的社会推理:标记主题建模
机译:患有NovelCOL4A1突变的新生儿的视神经发育不全Corp体发育不全白内障和异头畸形
机译:白质发育不全 - 胼callosum患有症状 - 智力残疾综合征