A Corneal Dystrophy Associated with Transforming Growth Factor β–Induced Gly623Asp Mutation

Author:

Auw-Haedrich Claudia,Agostini Hansjürgen,Clausen Ina,Reinhard Thomas,Eberwein Philipp,Schorderet Daniel F.,Gruenauer-Kloevekorn Claudia

Publisher

Elsevier BV

Subject

Ophthalmology

Reference12 articles.

1. Bilateral recurrence of granular corneal dystrophy in the grafts: a clinico-pathologic study;Witschel;Albrecht Von Graefes Arch Klin Exp Ophthalmol,1979

2. Corneal dystrophies in the light of modern molecular genetic research;Auw-Haedrich;Ophthalmologe,2002

3. Characteristic distribution of deposits in recurrent granular corneal dystrophy;Auw-Haedrich;Ger J Ophthalmol,1996

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

5. Survey of patients with granular, lattice, avellino, and Reis-Bucklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes;Afshari;Arch Ophthalmol,2001

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