A specific superoxide dismutase mutation is on the same genetic background in sporadic and familial cases of amyotrophic lateral sclerosis.

Lignende værker

• Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients.
  af: Jones, C T, et al.
  Udgivet: (1995)
• Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis.
  af: Hayward, C, et al.
  Udgivet: (1998)
• Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosis
  af: van Blitterswijk, Marka, et al.
  Udgivet: (2011)
• Immature Copper-Zinc Superoxide Dismutase and Familial Amyotrophic Lateral Sclerosis
  af: Seetharaman, Sai V., et al.
  Udgivet: (2009)
• Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity.
  af: Borchelt, D R, et al.
  Udgivet: (1994)