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Electrolytic removal of recurrence of granular corneal dystrophy

✍ Scribed by Mashima, Y; Kawashima, M; Yamada, M


Book ID
110035221
Publisher
Nature Publishing Group
Year
2003
Tongue
English
Weight
383 KB
Volume
17
Category
Article
ISSN
0950-222X

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Six autosomal dominant corneal dystrophies are caused by mutations in the TGFBI (BIGH3) gene on chromosome 5q31: three types of lattice corneal dystrophy (LCD), including type I and type IIIA, granular, Avellino (ACD), and Reis-Bucklers. Initially an exact genotype-phenotype correlation was reported