Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR.

Samankaltaisia teoksia

• Multiplex PCR for rapid detection of exonal deletions in patients of duchenne muscular dystrophy
  Tekijä: Singh, Ritu, et al.
  Julkaistu: (2006)
• Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients
  Tekijä: El Sherif, RM, et al.
  Julkaistu: (2007)
• Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
  Tekijä: Gangopadhyay, S B, et al.
  Julkaistu: (1992)
• Dystrophin hydrophobic regions in the pathogenesis of Duchenne and Becker muscular dystrophies
  Tekijä: Liang, Yingyin, et al.
  Julkaistu: (2015)
• Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.
  Tekijä: Florentin, L, et al.
  Julkaistu: (1995)