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42. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11. Jiao X; Sultana A; Garg P; Ramamurthy B; Vemuganti GK; Gangopadhyay N; Hejtmancik JF; Kannabiran C J Med Genet; 2007 Jan; 44(1):64-8. PubMed ID: 16825429 [TBL] [Abstract][Full Text] [Related]
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