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

Những quyển sách tương tự

• Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients.
  Bằng: Jones, C T, et al.
  Được phát hành: (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.
  Bằng: Hayward, C, et al.
  Được phát hành: (1998)
• Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosis
  Bằng: van Blitterswijk, Marka, et al.
  Được phát hành: (2011)
• Immature Copper-Zinc Superoxide Dismutase and Familial Amyotrophic Lateral Sclerosis
  Bằng: Seetharaman, Sai V., et al.
  Được phát hành: (2009)
• Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity.
  Bằng: Borchelt, D R, et al.
  Được phát hành: (1994)