A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract
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DOI: 10.1080/13816810.2017.1381977
Abstract: ABSTRACT Intoduction: Inherited cataract, opacification of the lens, is the most common worldwide cause of blindness in children. We aimed to identify the genetic cause of autosomal dominant (AD) posterior nuclear cataract in a four… read more here.
Keywords: site mutation; posterior nuclear; splice site; nuclear cataract ... See more keywords