Heavy-Chain Amyloidosis in TGFBI-Negative and Gelsolin-Negative Atypical Lattice Corneal Dystrophy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology
Reference15 articles.
1. Lattice corneal dystrophy. An inherited variety of amyloidosis restricted to the cornea.;Klintworth;Am J Pathol,1967
2. Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.;Aldave;Am J Ophthalmol,2004
3. Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied family.;Klintworth;Invest Ophthalmol Vis Sci,2004
4. Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy.;Meretoja;Clin Genet,1973
5. Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.;Maury;FEBS Lett,1990
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