Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12

Eitemau Tebyg

• Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy
  gan: Allen, Edwin H.A., et al.
  Cyhoeddwyd: (2016)
• Allele-specific siRNA silencing for the common Keratin 12 founder mutation in Meesmann epithelial corneal dystrophy
  gan: Allen, Edwin H. A., et al.
  Cyhoeddwyd: (2013)
• A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy
  gan: Sullivan, Lori S., et al.
  Cyhoeddwyd: (2007)
• A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy
  gan: Corden, L, et al.
  Cyhoeddwyd: (2000)
• Soft contact lens wear decreases epithelial microcysts in Meesmann's corneal dystrophy.
  gan: Bourne, W M
  Cyhoeddwyd: (1986)