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See Latest ArticlesMolecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies
Molecular Vision, 07/15/09
Kaur K et al. - Data suggests a potential susceptibility role for FOXC1 in generating severe eye pathologies. However, on the basis of these results, it is unlikely that FOXC1 mutation is a major causative factor of anophthalmia, microphthalmia, and coloboma.
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MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma
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