TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs' endothelial corneal dystrophy
Author:
Affiliation:
1. Department of Clinical Sciences/Ophthalmology Umeå University Umeå Sweden
2. Department of Medical Biosciences/Medical and Clinical Genetics Umeå University Umeå Sweden
Funder
Stiftelsen Kronprinsessan Margaretas Arbetsnämnd för Synskadade
Ögonfonden
Publisher
Wiley
Subject
Ophthalmology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/aos.15032
Reference55 articles.
1. Fuchs' endothelial dystrophy of the cornea
2. Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy
3. No Pathogenic Mutations Identified in theCOL8A1andCOL8A2Genes in Familial Fuchs Corneal Dystrophy
4. E2-2 Protein and Fuchs's Corneal Dystrophy
5. Fuchs' endothelial dystrophy: a fresh look at an aging disease
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1. Change in Visual Acuity of Patients With Fuchs Endothelial Corneal Dystrophy Over 1 Year;Cornea;2024-07-09
2. CTG18.1 expansion in transcription factor 4 (TCF4) in corneal graft failure: preliminary study;Cell and Tissue Banking;2024-01-11
3. DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy;Cellular and Molecular Life Sciences;2023-02-11
4. Podhod k klasterizacii pacientov po mikrochipovym dannym vnutri otdel'nyh lokusov s ispol'zovaniem kombinacij variantov;Вестник Российского государственного медицинского университета;2023-02
5. The approach to patient clustering based on the microchip data confined to distinct loci using the combinations of variants;Bulletin of Russian State Medical University;2023-02
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