Limitations of short-read NGS in detecting <i>RP1 Alu</i> insertions: a case emphasizing Sanger confirmation
<p>To assess the detectability of the pathogenic <i>RP1 Alu</i> insertion using the PrismGuide™ inherited retinal dystrophy (IRD) panel, which targets 82 IRD genes, and whole-exome sequencing (WES).</p> <p>A girl diagnosed with early-onset retinitis pigmentosa at age 7...
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2025
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