Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 gene

[1] Baratz KH(2010)E2-2 protein and Fuchs’s corneal dystrophy N Engl J Med 363 1016-1024

[2] Tosakulwong N(2012)A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy PLoS One 7 e49083-43

[3] Ryu E(2017)CTG18.1 expansion in TCF4 increases likelihood of transplantation in Fuchs corneal dystrophy Cornea 36 40-983

[4] Brown WL(1993)A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. The Huntington’s Disease Collaborative Research Group Cell 72 971-2039

[5] Branham K(1978)Corneal endothelial dystrophy. A study of 64 families Arch Ophthalmol 96 2036-378

[6] Chen W(2015)Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 (MMP19) in patients with cavitary optic disc anomaly (CODA) Hum Mutat 36 369-undefined

[7] Wieben ED(undefined)undefined undefined undefined undefined-undefined

[8] Aleff RA(undefined)undefined undefined undefined undefined-undefined

[9] Tosakulwong N(undefined)undefined undefined undefined undefined-undefined

[10] Butz ML(undefined)undefined undefined undefined undefined-undefined

[1] Baratz KH(2010)E2-2 protein and Fuchs’s corneal dystrophy N Engl J Med 363 1016-1024

[2] Tosakulwong N(2012)A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy PLoS One 7 e49083-43

[3] Ryu E(2017)CTG18.1 expansion in TCF4 increases likelihood of transplantation in Fuchs corneal dystrophy Cornea 36 40-983

[4] Brown WL(1993)A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. The Huntington’s Disease Collaborative Research Group Cell 72 971-2039

[5] Branham K(1978)Corneal endothelial dystrophy. A study of 64 families Arch Ophthalmol 96 2036-378

[6] Chen W(2015)Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 (MMP19) in patients with cavitary optic disc anomaly (CODA) Hum Mutat 36 369-undefined

[7] Wieben ED(undefined)undefined undefined undefined undefined-undefined

[8] Aleff RA(undefined)undefined undefined undefined undefined-undefined

[9] Tosakulwong N(undefined)undefined undefined undefined undefined-undefined

[10] Butz ML(undefined)undefined undefined undefined undefined-undefined