Unilateral Variant of Late-Onset Lattice Corneal Dystrophy With the Pro501Thr Mutation in the TGFBI Gene Without Deposits in the Unaffected Cornea Using Confocal Microscopy-Reference-Cited by-同舟云学术

Unilateral Variant of Late-Onset Lattice Corneal Dystrophy With the Pro501Thr Mutation in the TGFBI Gene Without Deposits in the Unaffected Cornea Using Confocal Microscopy

Published:2013-10 Issue:10 Volume:32 Page:1396-1398
ISSN:0277-3740
Container-title:Cornea
language:en
Short-container-title:

Author:

Kojima Yoshinao,Inoue Tomoyuki,Hori Yuichi,Maeda Naoyuki,Nishida Kohji

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology

Reference9 articles.

1. . Kerato-epithelin mutations in four 5q31-linked corneal dystrophies.;Munier;Nat Genet,1997

2. . Unilateral corneal lattice dystrophy.;Sridhar;Cornea,2001

3. . Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.;Hirano;Cornea,2001

4. . A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy.;Stewart;Ophthalmology,1999

5. . Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene.;Aldave;Mol Vis,2006

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