Deletions in the 5' region of dystrophin and resulting phenotypes.

Ítems similars

• Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.
  per: Abbs, S, et al.
  Publicat: (1992)
• Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.
  per: Sherratt, T G, et al.
  Publicat: (1993)
• Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion
  per: Gualandi, F, et al.
  Publicat: (2003)
• A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart.
  per: Muntoni, F, et al.
  Publicat: (1995)
• A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.
  per: Abbs, S, et al.
  Publicat: (1991)