OTX2 mutation associated with severe myopia in a Canadian family

Ophthalmic Genetics ◽

10.1080/13816810.2021.2015791 ◽

2021 ◽

pp. 1-3

Author(s):

Snow Wangding ◽

Samantha Colaiacovo ◽

Inas Makar ◽

Maha Saleh

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