Tmem63c mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia

HIGHLIGHTS

• who: Luis-Carlos Tu00e1bara and collaborators from the Medical Research Council Biology Unit, University of Cambridge, Cambridge , XY, UK 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 . . .
  

   

  

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