Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.

Benzer Materyaller

• Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin.
  Yazar:: Matsumura, K, ve diğerleri
  Baskı/Yayın Bilgisi: (1994)
• Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains 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)
• Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
  Yazar:: Gangopadhyay, S B, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype
  Yazar:: Witting, Nanna, ve diğerleri
  Baskı/Yayın Bilgisi: (2011)