Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy.

Lignende værker

• Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy
  af: Cohen, N, et al.
  Udgivet: (2004)
• A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.
  af: Ferlini, A, et al.
  Udgivet: (1998)
• The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy
  af: Neri, Marcella, et al.
  Udgivet: (2012)
• A case report: X-linked dystrophin gene mutation causing severe isolated dilated cardiomyopathy
  af: Lester, Geoffrey, et al.
  Udgivet: (2019)
• Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy
  af: Muntoni, F., et al.
  Udgivet: (1997)