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
PubMed
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.

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