Associated Papers
Novel mutations of the X-linked genes associated with early-onset high myopia in five Chinese families.
Zi F et al.
Bmc Medical Genomics, 2023
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism.
Wang Y et al.
Investigative Ophthalmology & Visual Science, 2023
Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1.
Li J et al.
Investigative Ophthalmology & Visual Science, 2015
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