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research article
Franceschetti Hereditary Recurrent Corneal Erosion
center dot PURPOSE: To describe new affected individuals of Franceschetti's original pedigree of hereditary recurrent erosion and to classify a unique entity called Franceschetti corneal dystrophy.
Type
research article
Web of Science ID
WOS:000304899300010
Authors
Lisch, Walter
•
Bron, Anthony J.
•
Munier, Francis L.
•
Schorderet, Daniel F.
•
Tiab, Leila
•
Lange, Clemens
•
Saikia, Parykshit
•
Reinhard, Thomas
•
Weiss, Jayne S.
•
Gundlach, Enken
Publication date
2012
Published in
Volume
153
Start page
1073
End page
1081
Subjects
Peer reviewed
REVIEWED
EPFL units
Available on Infoscience
June 29, 2012
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