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机译:患有α-亚替糖苷相关的肢体肌营养不良患者患者的纯合DPM3突变
Neuromuscular Reference Centre University Hospital St-Luc University of Louvain;
Neuromuscular Reference Centre University Hospital St-Luc University of Louvain;
Neuromuscular Reference Centre University Hospital St-Luc University of Louvain;
Department of Neurology Radboud University Medical Centre;
Translational Metabolic Laboratory Radboud University Medical Centre;
Department of Neurology Radboud University Medical Centre;
Analytic and Translational Genetics Unit Massachusetts General Hospital;
Analytic and Translational Genetics Unit Massachusetts General Hospital;
Analytic and Translational Genetics Unit Massachusetts General Hospital;
The John Walton Muscular Dystrophy Research Centre Institute of Genetic Medicine Newcastle;
The John Walton Muscular Dystrophy Research Centre Institute of Genetic Medicine Newcastle;
The John Walton Muscular Dystrophy Research Centre Institute of Genetic Medicine Newcastle;
The John Walton Muscular Dystrophy Research Centre Institute of Genetic Medicine Newcastle;
Limb girdle muscular dystrophy; Alpha-dystroglycan; Dolichol-P-mannose synthase; DPM3;
机译:勘探为“患有α-亚替糖苷相关的肢体肌营养不良症的患者纯合的DPM3突变”[神经肌肉障碍27/11(2017)1043-1046]
机译:患有α-亚替糖苷相关的肢体肌营养不良患者患者的纯合DPM3突变
机译:α-营养不良相关肢体带肌营养不良患者的纯合DPM3突变
机译:辅助机器人外骨骼帮助下肢带肌营养不良
机译:在Duchenne肌营养不良的年轻患者教育
机译:SGCD纯合性无意义突变(p.Arg97 *)在近亲家庭中引起2F型肢带型肌营养不良(LGMD2F)。
机译:肢体腰带肌营养不良型2I型:临床严重程度,组织病理学和糖基化α-当糖蛋白酶酸均纯合的常见FKRP突变患者之间无相关性
机译:验证功能性达到体积作为肌肉营养不良能力范围内的结果测量。