NUCLEAR GENE MUTATIONS AS THE CAUSE OF MITOCHONDRIAL COMPLEX III DEFICIENCY

Lignende værker

• Hypoxia Promotes Mitochondrial Complex I Abundance via HIF-1α in Complex III and Complex IV Deficient Cells
  af: Amy Saldana-Caboverde, et al.
  Udgivet: (2020-09-01)
• Characterising a homozygous two‐exon deletion in UQCRH: comparing human and mouse phenotypes
  af: Silvia Vidali, et al.
  Udgivet: (2021-11-01)
• A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia and bilateral basal ganglia lesions
  af: Laura eMelchionda, et al.
  Udgivet: (2014-11-01)
• Complex III deficiency due to an in-frame MT-CYB deletion presenting as ketotic hypoglycemia and lactic acidosis
  af: Mari Mori, et al.
  Udgivet: (2015-09-01)
• Mitochondrial proteomic profile of complex IV deficiency fibroblasts: rearrangement of oxidative phosphorylation complex/supercomplex and other metabolic pathways
  af: Karina Salvador-Severo, et al.
  Udgivet: (2017-05-01)