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See Latest ArticlesMutation analysis of congenital cataract in a Basotho family identified a new missense allele in CRYBB2
Molecular Vision, 07/31/09
Mothobi ME et al. – This study identified a missense mutation in CRYBB2 in a family of Basotho with autosomal dominant congenital cataract (ADCC). Authors believe this new missense allele is the probable causative molecular lesion for the observed phenotype in this family.
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MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma
Molecular Vision, 11/09/09
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Today in Lens and Cataract...keeping you current
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7 Infection Prevention Tips for Cataract Surgery
Outpatient Surgery, 11/11/09
Vitamin C supplements and the risk of age-related cataract: a population-based prospective cohort study in women
American Journal of Clinical Nutrition, 11/20/09
Late Increased Risk of Retinal Detachment after Cataract Extraction
American Journal of Ophthalmology, 10/30/09
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