A new mutation (A546T) of the βig-h3 gene responsible for a French lattice corneal dystrophy type IIIA-Reference-Cited by-同舟云学术

A new mutation (A546T) of the βig-h3 gene responsible for a French lattice corneal dystrophy type IIIA

Published:2000-02 Issue:2 Volume:129 Page:248-251
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Dighiero Paul,Drunat Severine,Ellies Pierre,D’Hermies François,Savoldelli Michèle,Legeais Jean-Marc,Renard Gilles,Delpech Marc,Grateau Gilles,Valleix Sophie

Publisher

Elsevier BV

Subject

Ophthalmology

Reference5 articles.

1. Lattice corneal dystrophy;Klintworth;Am J Pathol,1967

2. Lattice corneal dystrophy type IIIA;Stock;Arch Ophthalmol,1991

3. A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIA;Yamamoto;Am J Hum Genet,1998

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

5. Mutation hot spots in 5q31-linked corneal dystrophies;Korvatska;Am J Hum Genet,1998

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