Kerato-epithelin mutations in four 5q31-linked corneal dystrophies-Reference-Cited by-同舟云学术

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Kerato-epithelin mutations in four 5q31-linked corneal dystrophies

Published:1997-03 Issue:3 Volume:15 Page:247-251
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Munier Francis L.,Korvatska Elena,Djemaï Assia,Paslier Denis Le,Zografos Leonidas,Pescia Graziano,Schorderet Daniel F.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0397-247.pdf

Reference27 articles.

1. Møller, H.U. Inter-familial variability and intra-familial similarities of granular corneal dystrophy Groenouw type I with respect to biomicroscopical appearance and symptomatology. Acta Ophthalmol. 67, 669–677 (1989).

2. Klintworth, G.K. Lattice corneal dystrophy: an inherited variety of amyloidosis restricted to the cornea. Am. J. Pathol. 50, 371–399 (1967).

3. Folberg, R. et al. Clinically atypical granular corneal dystrophy with pathologic features of lattice-like amyloid deposits. Ophthalmology 95, 46–51 (1988).

4. Rosenwasser, G.O. et al. Phenotypic variation in combined granular-lattice (Avellino) corneal dystrophy. Arch. Ophthalmol. 111, 1546–1552 (1993).

5. Küchle, M. et al. Reevaluation of corneal dystrophies of Bowman's layer and the anterior stroma (Reis-Bücklers and Thiel-Behnke types): a light and electron microscopic study of eight corneas and a review of the literature. Cornea 14, 333–354 (1995).

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