Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level.

Biomed Res Int · 2015 · PMC4588027 · PMID 26451375

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highly significantno p-value reported

A genome-wide association study has identified a common biallelic deep intronic TCF4 single nucleotide polymorphism (SNP, rs613872; NG_011716.1 :g.50559C>A) as a highly significant risk factor for FECD [ 6 ].

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