Development of novel LOXL1 genotyping method and evaluation of LOXL1, APOE and MTHFR polymorphisms in exfoliation syndrome/glaucoma in a Greek population.

Mol Vis · 2013 · PMC3654845 · PMID 23687437

Europe PMC

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highly significantno p-value reported

Recently, genetic studies have demonstrated a highly significant association between XFS and sequence variants in the lysyl oxidase-like 1 ( LOXL1 ) gene coding for lysyl oxidase-like 1.

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