A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene

Antzeko izenburuak

• Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency
  nork: Jinru Zhang, et al.
  Argitaratua: (2022-07-01)
• Neutral lipid storage disease with myopathy presenting asymmetrical muscle weakness: a case report
  nork: Zhang, Jinru, et al.
  Argitaratua: (2020)
• Compound heterozygous mutations in electron transfer flavoprotein dehydrogenase identified in a young Chinese woman with late-onset glutaric aciduria type II
  nork: Ying Xue, et al.
  Argitaratua: (2017-09-01)
• Compound heterozygous mutations in electron transfer flavoprotein dehydrogenase identified in a young Chinese woman with late-onset glutaric aciduria type II
  nork: Xue, Ying, et al.
  Argitaratua: (2017)
• Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations
  nork: Liu, Xin-Yi, et al.
  Argitaratua: (2016)