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27. A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy. Yoon MK; Warren JF; Holsclaw DS; Gritz DC; Margolis TP Br J Ophthalmol; 2004 Jun; 88(6):752-6. PubMed ID: 15148206 [TBL] [Abstract][Full Text] [Related]
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