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Amanda N. Sadan
Amanda N. Sadan
UCL Institute of Ophthalmology
Medicine
Pathology
CRISPR
Genetics
TCF4
5
Papers
27
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Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?
2021
Genes
Lubica Dudakova
Pavlina Skalicka
Alice E. Davidson
Amanda N. Sadan
Monika Chylova
Helena Jahnová
Nicole Anteneová
Markéta Tesařová
Tomas Honzik
Petra Liskova
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CUGC for posterior polymorphous corneal dystrophy (PPCD)
2019
European Journal of Human Genetics
Alice E. Davidson
Nathaniel J. Hafford Tear
Lubica Dudakova
Amanda N. Sadan
Nikolas Pontikos
Alison J. Hardcastle
Stephen J. Tuft
Petra Liskova
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CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy–associated TCF4 triplet repeat
2019
Genetics in Medicine
Nathaniel J. Hafford Tear
Yu-Chih Tsai
Amanda N. Sadan
Beatriz Sanchez-Pintado
Christina Zarouchlioti
Geoffrey J. Maher
Petra Liskova
Stephen J. Tuft
Alison J. Hardcastle
Tyson A. Clark
Alice E. Davidson
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CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeat
2019
Investigative Ophthalmology & Visual Science
Alice E. Davidson
Nathaniel J. Hafford Tear
Yu-Chih Tsai
Amanda N. Sadan
Beatriz Sanchez-Pintado
Christina Zarouchlioti
Petra Liskova
Stephen J. Tuft
Tyson A. Clark
Alison J. Hardcastle
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