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Published on: August 15, 2019
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A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract
Vanita Berry1, Nikolas Pontikos1,2, Monica Albarca-Aguilera3
1a Genetics, UCL Institute of Ophthalmology , London , UK.
Ophthalmic Genetics
|October 18, 2017
Summary
A genetic mutation in the EPHA2 gene caused inherited posterior nuclear cataract, a leading cause of childhood blindness. This finding highlights further genetic diversity in congenital cataracts.
Area of Science:
- Genetics
- Ophthalmology
- Molecular Biology
Background:
- Inherited cataracts are a primary cause of childhood blindness globally.
- Posterior nuclear cataracts represent a significant subtype of pediatric visual impairment.
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