First Genetic Analysis of Lattice Corneal Dystrophy Type I in a Family from Bulgaria

2005 ◽  
Vol 15 (6) ◽  
pp. 804-808 ◽  
Author(s):  
E. Capoluongo ◽  
G. De benedetti ◽  
P. Concolino ◽  
M. Sepe ◽  
R. Ambu ◽  
...  
Keyword(s):  
Genetic Analysis ◽  
Corneal Dystrophy ◽  
Type I ◽  
Lattice Corneal Dystrophy

Transforming Growth Factor-β Induced Protein, βIG-H3, is Present in Degraded Form and Altered Localization in Lattice Corneal Dystrophy Type I

1998 ◽  
Vol 66 (6) ◽  
pp. 739-745 ◽  
Author(s):  
LILI TAKÁCS ◽  
PÉTER BOROSS ◽  
JÓZSEF TÖZSÉR ◽  
LÁSZLÓ MÓDIS JR ◽  
GÁBOR TÓTH ◽  
...  
Keyword(s):  
Growth Factor ◽  
Transforming Growth Factor ◽  
Transforming Growth Factor Β ◽  
Corneal Dystrophy ◽  
Type I ◽  
Lattice Corneal Dystrophy

Lattice Corneal Dystrophy Type I and Variants

2009 ◽  
pp. 1143-1145
Author(s):  
Alexander K. C. Leung ◽  
William Lane M. Robson ◽  
Carsten Büning ◽  
Johann Ockenga ◽  
Janine Büttner ◽  
...  
Keyword(s):  
Corneal Dystrophy ◽  
Type I ◽  
Lattice Corneal Dystrophy

Leu518Pro mutation of the βig-h3 gene causes lattice corneal dystrophy type I

1999 ◽  
Vol 128 (1) ◽  
pp. 104-106 ◽  
Author(s):  
Shinichiro Endo ◽  
Nguyen Thanh Ha ◽  
Keiko Fujiki ◽  
Yoshihiro Hotta ◽  
Kiyoo Nakayasu ◽  
...  
Keyword(s):  
Corneal Dystrophy ◽  
Type I ◽  
Lattice Corneal Dystrophy

Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis

2004 ◽  
Vol 137 (3) ◽  
pp. 586-588 ◽  
Author(s):  
Shigeo Yoshida ◽  
Ayako Yoshida ◽  
Shintaro Nakao ◽  
Aki Emori ◽  
Takao Nakamura ◽  
...  
Keyword(s):  
Mutational Analysis ◽  
Corneal Dystrophy ◽  
Type I ◽  
Lattice Corneal Dystrophy

A Novel H572R Mutation in the Transforming Growth Factor-β-Induced Gene in a Thai Family with Lattice Corneal Dystrophy Type I

2006 ◽  
Vol 50 (5) ◽  
pp. 403-408 ◽  
Author(s):  
La-ongsri Atchaneeyasakul ◽  
◽  
Binoy Appukuttan ◽  
Sarinee Pingsuthiwong ◽  
Pa-thai Yenchitsomanus ◽  
...  
Keyword(s):  
Growth Factor ◽  
Transforming Growth Factor ◽  
Transforming Growth Factor Β ◽  
Corneal Dystrophy ◽  
Type I ◽  
Lattice Corneal Dystrophy

Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I

2005 ◽  
Vol 49 (2) ◽  
pp. 84-88 ◽  
Author(s):  
Xin Tian ◽  
Keiko Fujiki ◽  
Wei Wang ◽  
Akira Murakami ◽  
Peiying Xie ◽  
...  
Keyword(s):  
Novel Mutation ◽  
Corneal Dystrophy ◽  
Chinese Family ◽  
Type I ◽  
Lattice Corneal Dystrophy ◽  
Tgfbi Gene
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