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APA Citation
Berry, V., Ionides, A., Pontikos, N., Moghul, I., Moore, A., Cheetham, M., & Michaelides, M. (2018). whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract. Eye, 32, 1661–1668. http://access.bl.uk/ark:/81055/vdc_100084799062.0x000114