Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1.

Nat Commun · 2017 · PMC5457519 · PMID 28534485

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highly significantno p-value reported

Discussion Genetic and pathogenetic analyses have confirmed a highly significant and direct role for LOXL1 in the pathophysiology of PEX syndrome and its associated ocular and systemic complications.

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