Adult‐onset myoclonus ataxia associated with the mitochondrial m.8993T>C “NARP” mutation

Lignende værker

• Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'.
  af: Fryer, A, et al.
  Udgivet: (1994)
• Episodic ataxia and hemiplegia caused by the 8993T→C mitochondrial DNA mutation
  af: Craig, K, et al.
  Udgivet: (2007)
• The frequency of mtDNA 8994 polymorphism and detection of the NARP 8993 mutation
  af: Gray, R, et al.
  Udgivet: (2002)
• Mitochondrial Donation — How Many Women Could Benefit?
  af: Gorman, Gráinne S., et al.
  Udgivet: (2015)
• Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation.
  af: de Coo, I. F., et al.
  Udgivet: (1996)