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Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract https://t.co/405GT8YEaq https://t.co/hwWEjnqnrp
Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract https://t.co/405GT8YEaq https://t.co/hwWEjnqnrp
Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract https://t.co/wxWJAteozR
New Research: Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract: Congenital hereditary cataract is genetically heterogeneous and the leading cause of visual impairment in children.… https://t.co/GxXQauxzoP