Barely Significant
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Toward an elucidation of the molecular genetics of inherited retinal degenerations.

Hum Mol Genet · 2017 · PMC5886474 · PMID 28510639

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highly significantno p-value reported
-is-real-version no pmc-prop-is-scanned-article no pmc-prop-preprint no pmc-prop-in-epmc yes pmc-license-ref CC BY Genetic Heterogeneity in IRDs Inherited retinal degenerations (IRDs) represent the most frequent cause of visual dysfunction in those of working age, such conditions therefore having a highly significant impact on quality of life and health economics.

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