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See Latest ArticlesMutational screening of VSX1 in keratoconus patients from the European population
Eye, 09/21/09
Dash DP et al. – VSX1has a minor role in keratoconus pathogenesis. The pathogenicity of p.G160D remains controversial and this change may represent a rare polymorphism or genetic modifier. Further evidence is provided that the previously reported variant, p.D144E, is a polymorphism.
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