A novel p.R890C mutation in EPHA2 gene associated with progressive childhood posterior cataract in a Chinese family
<b>AIM:</b>To identify the genetic defect in a Chinese family with bilateral progressive childhood posterior cataract.<b>METHODS:</b> A two-generation family was recruited in this study. Family history and clinical data were recorded. All reported candidate genes associated w...
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Format: | Article |
Language: | English |
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Press of International Journal of Ophthalmology (IJO PRESS)
2013-02-01
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Series: | International Journal of Ophthalmology |
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Online Access: | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580246/ |