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Unveiling XXYLT1 as a Novel Mendelian Gene in Inherited Retinal Dystrophy: Insights from an Integrated GWAS Approach
newsXXYLT1inherited retinal dystrophy

Unveiling XXYLT1 as a Novel Mendelian Gene in Inherited Retinal Dystrophy: Insights from an Integrated GWAS Approach

By MedXY|Aug 4, 2026

A genome-wide association study in Finnish and UK cohorts identifies XXYLT1 as a novel gene implicated in Mendelian inherited retinal dystrophy, expanding genetic understanding and clinical diagnostic tools for this blinding condition.

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