Tmem63c mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia

HIGHLIGHTS

• who: Luis-Carlos Tábara et al. from the (UNIVERSITY) have published the research: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia, in the Journal: (JOURNAL)
• what: Horseradish peroxidaseconjugated anti-rabbit and anti-mouse IgG (GE Healthcare) were used as secondary antibodies (1:3000). for all the experiments presented in the figures are displayed in Supplementary Fig 4. The authors aimed to elucidate the cellular distribution of TMEM63C. One limitation of this study has been that the authors have been unable to obtain patientderived fibroblasts to investigate the effects of TMEM63C gene . . .
  

   

  

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