A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy

Lignende værker

• A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy
  af: Corden, L, et al.
  Udgivet: (2000)
• Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12
  af: Hassan, H, et al.
  Udgivet: (2013)
• 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)
• 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)
• Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy.
  af: Nishida, K, et al.
  Udgivet: (1997)