Clinical and Genetic Aspects of the TGFBI-associated Corneal Dystrophies-Reference-Cited by-同舟云学术

Clinical and Genetic Aspects of the TGFBI-associated Corneal Dystrophies

Published:2014-10 Issue:4 Volume:12 Page:234-251
ISSN:1542-0124
Container-title:The Ocular Surface
language:en
Short-container-title:The Ocular Surface

Author:

Lakshminarayanan R.,Chaurasia Shyam S.,Anandalakshmi Venkatraman,Chai Shu-Ming,Murugan Elavazhagan,Vithana Eranga N.,Beuerman Roger W.,Mehta Jodhbir S.

Funder

Duke-NUS/ SingHealth Academic Medicine Research Institute

Publisher

Elsevier BV

Subject

Ophthalmology

Reference132 articles.

1. Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy;Irvine;Nat Genet,1997

2. A novel keratin 12 mutation in German kindred with Meesmann's corneal dystrophy;Corden;Br Ophthalmol,2000

3. A previously unrecognized form of subepithelial corneal dystrophy inherited as an autosomal dominant;Behnke;Ger Med Mon,1967

4. Reevaluation of corneal dystrophies of Bowman's layer and the anterior stroma (Reis-Bucklers and Thiel-Behnke types): A light and electron microscopic study of eight corneas and a review of the literature;Kuchle;Cornea,1995

5. Lattice corneal dystrophy- an inherited variety of amyloidosis restricted to the cornea;Klintworth;Am J Pathol,1967

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