A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy

Lignende værker

• Allele-specific siRNA silencing for the common Keratin 12 founder mutation in Meesmann epithelial corneal dystrophy
  af: Allen, Edwin H. A., et al.
  Udgivet: (2013)
• A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy
  af: Irvine, A D, et al.
  Udgivet: (2002)
• Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy
  af: Allen, Edwin H.A., et al.
  Udgivet: (2016)
• Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann`s corneal dystrophy in a German family
  af: Clausen, Ina, et al.
  Udgivet: (2010)
• A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy
  af: Sullivan, Lori S., et al.
  Udgivet: (2007)