The low allele frequency or absence of the rs11720822 [T] variant in PDIA5 and the rs387907358 [T] and rs77542162 [G] variants in WNT1 and ABCA6 , respectively, among KC patients of Saudi origin suggests that these particular variants might not be significant risk factors for KC in Saudi individuals.
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Gender-specific association of <i>STON2</i> rs2371597 polymorphism in keratoconus patients of Saudi origin.
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