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HARVARD Citation
Berry, V. et al. (2018). A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract. Ophthalmic genetics. pp. 236-241. [Online].
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Berry, V. et al. (2018). A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract. Ophthalmic genetics. pp. 236-241. [Online].