Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy.

Podobne zapisy

• Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy.
  od: Chang, P L, i wsp.
  Wydane: (1983)
• Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.
  od: Chang, P L, i wsp.
  Wydane: (1980)
• High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophy.
  od: Kreysing, J, i wsp.
  Wydane: (1993)
• METACHROMATIC LEUKODYSTROPHY: ARYLSULFATASE-A DEFICIENCY IN SKIN FIBROBLAST CULTURES
  od: Porter, Myna T., i wsp.
  Wydane: (1969)
• Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy.
  od: Gieselmann, V, i wsp.
  Wydane: (1991)