Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype

Benzer Materyaller

• A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene
  Yazar:: Zimowski, Janusz G., ve diğerleri
  Baskı/Yayın Bilgisi: (2017)
• Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
  Yazar:: Gangopadhyay, S B, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR.
  Yazar:: Covone, A E, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.
  Yazar:: Matsumura, K, ve diğerleri
  Baskı/Yayın Bilgisi: (1993)
• Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients
  Yazar:: El Sherif, RM, ve diğerleri
  Baskı/Yayın Bilgisi: (2007)