https://www.selleckchem.com/pr....oducts/Methazolaston
The c.1102CT, p.(Gln368Ter) variant in the myocilin (MYOC) gene is a known risk allele for glaucoma. It is the most common MYOC risk variant for glaucoma among individuals of European ancestry, and its prevalence is highest in Finland. Furthermore, exfoliation syndrome has high prevalence in Scandinavia, making the Finnish population ideal to study the association of the variant with different types of glaucoma. To examine the association and penetrance of MYOC p.(Gln368Ter) (rs74315329) variant with different types of glauco
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