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Polymorphisms of the Homologous Recombination Gene RAD51 in Keratoconus and Fuchs Endothelial Corneal Dystrophy

Purpose. We investigated the association between genotypes and haplotypes of the c.-61G>T (rs 1801320) and c.-98G>C (rs 1801321) polymorphisms of the RAD51 gene and the occurrence of keratoconus (KC) and Fuchs endothelial corneal dystrophy (FECD) in dependence on some environmental factors. Me...

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Bibliografiset tiedot
Päätekijät: Synowiec, Ewelina, Wojcik, Katarzyna A., Izdebska, Justyna, Binczyk, Ewelina, Blasiak, Janusz, Szaflik, Jerzy, Szaflik, Jacek P.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi Publishing Corporation 2013
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3809973/
https://ncbi.nlm.nih.gov/pubmed/24223453
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/851817
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