A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions

Lignende værker

• A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions
  af: Rouzier, Cécile, et al.
  Udgivet: (2017)
• Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases
  af: Plutino, Morgane, et al.
  Udgivet: (2018)
• MT-CYB deletion in an encephalomyopathy with hyperintensity of middle cerebellar peduncles
  af: Chaussenot, Annabelle, et al.
  Udgivet: (2018)
• Coenzyme Q(10) defects may be associated with a deficiency of Q(10)-independent mitochondrial respiratory chain complexes
  af: Fragaki, Konstantina, et al.
  Udgivet: (2016)
• A novel variant m.8561C>T in the overlapping region of MT-ATP6 and MT-ATP8 in a child with early-onset severe neurological signs
  af: Fragaki, Konstantina, et al.
  Udgivet: (2019)