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Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract
Berry, Vanita, Ionides, Alexander C. W., Pontikos, Nikolas, Moghul, Ismail, Moore, Anthony T., Cheetham, Michael E., Michaelides, MichelLanguage:
english
Journal:
Eye
DOI:
10.1038/s41433-018-0154-8
Date:
June, 2018
File:
PDF, 1.04 MB
english, 2018