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Purpose
To detect variants in 17 known potentially causative genes for non‐syndromic myopia in 67 Tujia Chinese patients with early‐onset high myopia (eo‐HM).
Methods
DNA from 67 unrelated patients with early onset (<7 years old) high myopia (refraction error ≤ −6.00D or axial length > 26 mm) were subjected to whole‐exome sequencing (WES). Variants in 17 candidate genes were analysed by multistep...
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