The arylsulphatase A gene and molecular genetics of metachromatic leucodystrophy.

Samankaltaisia teoksia

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