Condition: Corneal Dystrophy, Lattice Type IIIA
rs121909212
in
TGFBI
gene and
Corneal Dystrophy, Lattice Type IIIA
PMID 15790870
2005 Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.
PMID 9497262
1998 A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA.