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XXYLT1

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

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

Posted by By MedXY 08/04/2026
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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