Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients.

Ítems similars

• A specific superoxide dismutase mutation is on the same genetic background in sporadic and familial cases of amyotrophic lateral sclerosis.
  per: Hayward, C., et al.
  Publicat: (1996)
• Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.
  per: Pramatarova, A, et al.
  Publicat: (1995)
• Posttranslational Modifications in Cu,Zn-Superoxide Dismutase and Mutations Associated with Amyotrophic Lateral Sclerosis
  per: FURUKAWA, YOSHIAKI, et al.
  Publicat: (2006)
• 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.
  per: Hayward, C, et al.
  Publicat: (1998)
• Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity.
  per: Borchelt, D R, et al.
  Publicat: (1994)