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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
PubMed

Keywords:
Congenital cataractEPHA2whole genome sequencing

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