The arylsulphatase A gene and molecular genetics of metachromatic leucodystrophy.

Míreanna Comhchosúla

• Molecular analysis of the arylsulphatase A gene in late infantile metachromatic leucodystrophy patients and healthy subjects from Italy.
  le: Regis, S, et al.
  Foilsithe: (1996)
• Metachromatic leucodystrophy in three families from Nova Scotia, Canada: a recurring mutation in the arylsulphatase A gene.
  le: Coulter-Mackie, M B, et al.
  Foilsithe: (1997)
• Restoration of arylsulphatase A activity in human-metachromatic-leucodystrophy fibroblasts via retroviral-vector-mediated gene transfer.
  le: Rommerskirch, W, et al.
  Foilsithe: (1991)
• A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophy.
  le: Zlotogora, J, et al.
  Foilsithe: (1994)
• Frequency of arylsulphatase A pseudodeficiency associated mutations in a healthy population.
  le: Barth, M L, et al.
  Foilsithe: (1994)