2024-03-28T16:35:36Z
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oai:serval.unil.ch:BIB_A4533DEABE1A
2024-03-23T02:47:04Z
serval:BIB_A4533DEABE1A
Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin
10.1167/iovs.04-1319
000227908900004
15790870
Stix
B.
author
Leber
M.
author
Bingemer
P.
author
Gross
C.
author
Ruschoff
J.
author
Fandrich
M.
author
Schorderet
D. F.
author
Vorwerk
C. K.
author
Zacharias
M.
author
Roessner
A.
author
Rocken
C.
author
article
2005-04
Investigative Ophthalmology and Visual Science
0146-0404
journal
46
4
1133-9
Adult
Amyloid/*metabolism
Amyloidosis, Familial/*genetics/metabolism/pathology
Blotting, Western
Codon
Cornea/*metabolism/pathology
Corneal Dystrophies, Hereditary/*genetics/metabolism/pathology
Electrophoresis, Polyacrylamide Gel
Exons
Extracellular Matrix Proteins/*genetics/metabolism
Female
Gene Amplification
Humans
Keratoplasty, Penetrating
Male
Middle Aged
Pedigree
*Point Mutation
Polymerase Chain Reaction
Transforming Growth Factor beta/*genetics/metabolism
60_published
true
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Apr