Cite
HARVARD Citation
Berry, V. et al. (2018). Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract. Eye. pp. 1661-1668. [Online].
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Berry, V. et al. (2018). Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract. Eye. pp. 1661-1668. [Online].