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22. Molecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies. Alka K; Casey JR Hum Mutat; 2018 May; 39(5):676-690. PubMed ID: 29327391 [TBL] [Abstract][Full Text] [Related]
23. Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India. Gupta R; Kumawat BL; Paliwal P; Tandon R; Sharma N; Sen S; Kashyap S; Nag TC; Vajpayee RB; Sharma A Mol Vis; 2015; 21():1252-60. PubMed ID: 26622166 [TBL] [Abstract][Full Text] [Related]
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