Cite
HARVARD Citation
Lin, M. et al. (2020). A novel c.287G>T NDP missense mutation in a Chinese family with Norrie disease. Ophthalmic genetics. pp. 338-340. [Online].
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Lin, M. et al. (2020). A novel c.287G>T NDP missense mutation in a Chinese family with Norrie disease. Ophthalmic genetics. pp. 338-340. [Online].