机译:由于DPM3基因的新致病变体,扩张心肌病和肢体肌营养不良 - Dystrophy
Hosp Civils Lyon Electroneuromyog &
Neuromuscular Dept Lyon France;
Hop Raymond Poincare Ctr Reference Malad Neuromusculaires Nord Est Ile Serv Neurol Garches;
Hosp Civils Lyon Electroneuromyog &
Neuromuscular Dept Lyon France;
Hosp Civils Lyon Dept Neuropathol Lyon France;
UPMC Univ Paris 06 Sorbonne Univ Grp Hosp Univ La Pitie Salpetriere Myol Inst Neuromuscular;
Hop Xavier Bichat AP HP Biochem Paris France;
Hop Xavier Bichat AP HP Biochem Paris France;
Hop Xavier Bichat AP HP Biochem Paris France;
Hop Xavier Bichat AP HP Biochem Paris France;
Hosp Civils Lyon Dept Mol Endocrinol &
Rare Dis Lyon France;
Hosp Civils Lyon Dept Mol Endocrinol &
Rare Dis Lyon France;
UPMC Univ Paris 06 Sorbonne Univ Grp Hosp Univ La Pitie Salpetriere Myol Inst Neuromuscular;
Alpha-dystroglycanopathies; Congenital disorders of glycosylation; Dilated cardiomyopathy; Dolichol-P-mannose (DPM) synthase subunit 3 (DPM3); Limb-girdle muscular dystrophy;
机译:由于DPM3基因的新致病变体,扩张心肌病和肢体肌营养不良 - Dystrophy
机译:LMNA基因第1外显子的R25G突变与扩张型心肌病和肢带型肌营养不良1B相关
机译:在SIB对中引起肢体肌营养不良 - Dystrophy的新型化合物杂合性突变
机译:扩散和理想的MRI技术,表征肢体肌营养不良症
机译:系统综述及萨法利亚斯坦坦斯在棘突式截断变体引起的家族性扩张心肌病管理中的应用研究和拟议研究研究
机译:肢体腰带肌营养不良型2I型和扩张心肌病的产科管理
机译:在SIB对中引起LIMB-LDLE肌营养不良 - Dystrophy的新型化合物杂合酶突变