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Noncoding U4/U6 RNA Variants Pinpointed as Cause of Retinitis Pigmentosa

The discovery elevates small nuclear RNA genes to clinically relevant targets for retinal disease diagnostics.

Study of 16p12.1 Families in Cell Shows Secondary Variants Shape Disease

Largest Genetic Map of Human Metabolism Charts 29,824 DNA–Metabolite Links

Genome-Wide Study Confirms Genetic Basis of Stuttering, Identifies 57 Risk Loci