Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Vision and ZNF469[original query] |
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Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy. PloS one 2012 7 (10): e46742. Igo Robert P, Kopplin Laura J, Joseph Peronne, Truitt Barbara, Fondran Jeremy, Bardenstein David, Aldave Anthony J, Croasdale Christopher R, Price Marianne O, Rosenwasser Miriam, Lass Jonathan H, Iyengar Sudha K, |
Mutations in the zinc finger protein gene, ZNF469, contribute to the pathogenesis of keratoconus. Investigative ophthalmology & visual science 2014 Sep 55 (9): 5629-35. Vincent Andrea L, Jordan Charlotte A, Cadzow Murray J, Merriman Tony R, McGhee Charles |
Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus. Investigative ophthalmology & visual science 2015 1 56 (1): 578-86. Davidson Alice E, Borasio Edmondo, Liskova Petra, Khan Arif O, Hassan Hala, Cheetham Michael E, Plagnol Vincent, Alkuraya Fowzan S, Tuft Stephen J, Hardcastle Alison |
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