Insight into Pathogenic Mechanism Underlying the Hereditary Cataract Caused by βB2-G149V Mutation
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DOI: 10.3390/biom13050864
Abstract: Congenital cataracts account for approximately 5–20% of childhood blindness worldwide and 22–30% of childhood blindness in developing countries. Genetic disorders are the primary cause of congenital cataracts. In this work, we investigated the underlying molecular… read more here.
Keywords: crystallin; g149v mutation; congenital cataracts; mechanism ... See more keywords