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.