A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA.

Ítems similars

• Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p.
  per: Tsujikawa, M, et al.
  Publicat: (1998)
• Homogeneity of kerato-epithelin codon 124 mutations in Japanese patients with either of two types of corneal stromal dystrophy.
  per: Mashima, Y, et al.
  Publicat: (1997)
• Corneal guttata associated with the corneal dystrophy resulting from a βig-h3 R124H mutation
  per: Akimune, C., et al.
  Publicat: (2000)
• Lattice Familial Corneal Dystrophy
  per: Ramsay, Robert M.
  Publicat: (1957)
• Ophthaproblem. Lattice corneal dystrophy.
  per: Cheung, J., et al.
  Publicat: (2001)