A Simple DNA Chip for Diagnosis of Most Common Corneal Dystrophies Caused by ßigh3 Gene Mutations
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Sang Yup Lee | So Young Yoo | Tae-im Kim | Eng Kweon Kim | Ki Chang Keum | Nae Choon Yoo | Won Min Yoo | K. Keum | S. Yoo | S. Y. Lee | Tae-im Kim | N. Yoo | W. Yoo | E. K. Kim
[1] R. D. Stulting,et al. Avellino corneal dystrophy after LASIK. , 2004, Ophthalmology.
[2] A. Ridgway,et al. Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene , 2000 .
[3] A. Murakami,et al. H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese people , 2003, The British journal of ophthalmology.
[4] A. Aldave,et al. Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene. , 2004, American journal of ophthalmology.
[5] K. Fujiki,et al. Late-onset Form of Lattice Corneal Dystrophy Caused by Leu527Arg Mutation of the TGFBI Gene , 2001, Cornea.
[6] N. Afshari,et al. Polymorphic corneal amyloidosis: a disorder due to a novel mutation in the transforming growth factor beta-induced (BIGH3) gene. , 2004, Ophthalmology.
[7] S. Yoshida,et al. Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis. , 2004, American journal of ophthalmology.
[8] M. Yamada,et al. Varied appearance of cornea of patients with corneal dystrophy associated with R124H mutation in the BIGH3 gene. , 1999, Cornea.
[9] W. Spencer,et al. A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I. , 2003, American journal of ophthalmology.
[10] P. Boelle,et al. Clinical outcome of eight BIGH3-linked corneal dystrophies. , 2002, Ophthalmology.
[11] W. Culbertson,et al. Mutation hot spots in 5q31-linked corneal dystrophies. , 1998, American journal of human genetics.
[12] R. Steinert,et al. Survey of patients with granular, lattice, avellino, and Reis-Bücklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes. , 2001, Archives of ophthalmology.
[13] K. Fujiki,et al. Corneal amyloidosis caused by Leu518Pro mutation of βig-h3 gene , 2000 .
[14] M. Delpech,et al. Histologic phenotype-genotype correlation of corneal dystrophies associated with eight distinct mutations in the TGFBI gene. , 2001, Ophthalmology (Rochester, Minn.).
[15] G. Klintworth. The molecular genetics of the corneal dystrophies--current status. , 2003, Frontiers in bioscience : a journal and virtual library.
[16] L. Ficker,et al. BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDI , 2004, Eye.
[17] K. Keum,et al. Development of a DNA chip for the diagnosis of the most common corneal dystrophies caused by mutations in the βigh3 gene , 2007, British Journal of Ophthalmology.
[18] M. W. Mueller,et al. Microarray-Based Identification of Bacteria in Clinical Samples by Solid-Phase PCR Amplification of 23S Ribosomal DNA Sequences , 2004, Journal of Clinical Microbiology.