A recurrent splice-site mutation in EPHA2...

Ophthalmic Genetics 2017 / 10

A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract

Berry, Vanita, Pontikos, Nikolas, Albarca-Aguilera, Monica, Plagnol, Vincent, Massouras, Andreas, Prescott, DeQuincy, Moore, Anthony T., Arno, Gavin, Cheetham, Michael E., Michaelides, Michel
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Language:
english
Journal:
Ophthalmic Genetics
DOI:
10.1080/13816810.2017.1381977
Date:
October, 2017
File:
PDF, 1.13 MB
english, 2017
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