A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.

Những quyển sách tương tự

• Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy.
  Bằng: Muntoni, F, et al.
  Được phát hành: (1995)
• The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy
  Bằng: Neri, Marcella, et al.
  Được phát hành: (2012)
• Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy
  Bằng: Cohen, N, et al.
  Được phát hành: (2004)
• Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy
  Bằng: Muntoni, F., et al.
  Được phát hành: (1997)
• A case report: X-linked dystrophin gene mutation causing severe isolated dilated cardiomyopathy
  Bằng: Lester, Geoffrey, et al.
  Được phát hành: (2019)